SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11279 | snp | G/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610721 | TAGCATGTCTCAACA[G/T]CCAGCCTGAGGTAGG | 6468 |
rs14467 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610801 | GGTTTCAAAGCAAAA[C/T]CAGGCCACAGTGCCC | 6468 |
rs888505 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671463 | AAGAATAGCAAGTTT[A/G]TTTGAGATACTGGGT | 6468 |
rs1035291 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677087 | caccaacaatgtagg[A/C]gagtttcTTATTGGT | 6468 |
rs1468973 | snp | G/T | 0.326506 | 0.238006 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632233 | TGGGTTGAGAGAGGG[G/T]TGCGTGTGTGTGTGT | 6468 |
rs1544720 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659496 | GCTTAGTTTTCCCAC[C/T]GCTGGTCTCTAGGTA | 6468 |
rs1549065 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653151 | TCCCTCTCTCCCTGA[C/T]GTGCAGTCATGTCTG | 6468 |
rs2080698 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654723 | AAGGATGACACAGAT[A/G]TACATTTATGGAACC | 6468 |
rs2080699 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654599 | TGGATTTCTGTTGAT[A/G]TTTACTTACTTTTTA | 6468 |
rs3095789 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627783 | AGTCCATTCATGGAA[A/G]CTTGGCCTTTGCTTC | 6468 |
rs3095790 | snp | A/C | 0.336839 | 0.235922 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626924 | GATTTACATCCCCAC[A/C]CCACCCTCATCCCTG | 6468 |
rs3095791 | snp | A/G | 0.19646 | 0.2442 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624079 | tgtctgtctgtgtct[A/G]tgtgtgtctagtcct | 6468 |
rs3127230 | snp | C/T | 0.381503 | 0.21262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632746 | CCCCTTAAACAACTG[C/T]TCCATGTGCTCCTAA | 6468 |
rs3127255 | snp | C/T | 0.332106 | 0.236133 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610477 | ACAGGTGACCCTCCA[C/T]ACCCCAAAGGGTAAG | 6468 |
rs3127256 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615217 | GAGCCTTGGCTGTTG[C/G]ACAGCTTGTGTGGGA | 6468 |
rs3127257 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620339 | TCTGGGAAAGACAGC[G/T]CTAGAGAGTCATCCT | 6468 |
rs3127258 | snp | C/T | 0.334412 | 0.235318 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623403 | aaacataaataaata[C/T]agattttaaaaaaga | 6468 |
rs3758559 | snp | A/G | 0.322483 | 0.239262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685475 | CTTAGTGTCTGATAG[A/G]AATCCCTGTAAAATT | 6468 |
rs3901642 | snp | A/C | 0.322483 | 0.239262 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669141 | GTAACTCACACAATC[A/C]TCCCATCCCCCACCC | 6468 |
rs3902130 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668236 | ACTTCTGATTCCCCA[A/G]TGTAAAGTTGGCTGG | 6468 |
rs3925644 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669997 | gaggctgaggcgggt[A/G]gatcatgaggtcagg | 6468 |
rs3925645 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669946 | aacacagcaaaaccc[C/T]gtgtctactaaaaat | 6468 |
rs3925646 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669815 | gtgagctgatattgc[A/G]ccactgcactccagc | 6468 |
rs4081695 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666924 | GAAACAAAAAAAGAA[C/T]GAAAAAAAAACCACC | 6468 |
rs4081696 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670705 | ACTCATAAGAAAGAA[C/T]AGAGAAATAAAGAAG | 6468 |
rs4244347 | snp | A/C | 0.431473 | 0.171952 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692888 | TGGCAGAGCCTAATA[A/C]AGTGTAAAACAGTAA | 6468 |
rs4326724 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673991 | GACTTCTCATGGGTA[C/T]GCAGAGCTTACAAAA | 6468 |
rs4917943 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664468 | ACATCCCCTCATATT[C/T]TCCATGAGGAGTCCA | 6468 |
rs4917944 | snp | A/G | 0.377977 | 0.21476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664553 | GGAGGGGAACTGAAG[A/G]TGGTCATTGAGGGCA | 6468 |
rs4919563 | snp | A/G | 0.381308 | 0.21274 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637159 | gaggctgaggcgggc[A/G]gatcacgaggtcagg | 6468 |
rs4919564 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642659 | ACCAAATTCTACCTC[C/T]GAAGCCTCCTTGGTA | 6468 |
rs4919565 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654710 | TATGACATCTTTTGG[G/T]TCCATAAATGTATAT | 6468 |
rs4919566 | snp | A/C | 0.195526 | 0.243993 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655128 | TGCCACCATGCCTGG[A/C]CTATTTATGTGTTCT | 6468 |
rs4919567 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655148 | ttatgtgttcttaat[A/G]taagtctttgtacat | 6468 |
rs4919571 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664113 | GAACTCAAAGTAAAG[G/T]AAGAAAGGAAAGAAG | 6468 |
rs4919572 | snp | A/G | 0.323197 | 0.239044 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664167 | TGCTTTCTCTCAGTC[A/G]TGAGGACCTCAAATT | 6468 |
rs4919573 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666505 | AAAGAAGCTGAAGGG[A/C]CTAAACGAAGTGGGT | 6468 |
rs4919578 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670909 | AGTCCCTAGCTCAGA[A/T]GTCTTGCAAAGAGAT | 6468 |
rs4919584 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688096 | GGGGCAGGAGAAGGC[A/G]GAGGAATGAACTGGC | 6468 |
rs5787442 | in-del | -/AG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691401 | CCAGAAAACCCGAGC[-/AG]TGACCCTGCTCTTTA | 6468 |
rs6584435 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643518 | GGATGCCGCAGGCAT[A/G]TGCACGCTTTGCATT | 6468 |
rs6584436 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646788 | TTTTACATTTTGGTT[C/T]TGGGGTATTTAGTTG | 6468 |
rs6584437 | snp | A/T | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648486 | TTCTGGGGACTGATT[A/T]TACTTTGAACATGAG | 6468 |
rs6584438 | snp | C/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655677 | GCAGCTGCAACAAGG[C/T]GGAAAATAGCAGGAG | 6468 |
rs6584439 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656827 | ATATCCTATAAGGTT[C/G]TCTCTTGTTACTTGA | 6468 |
rs6584441 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666960 | TCTAGGGCTGGGCAC[A/G]GTGGCTCACAACTGT | 6468 |
rs6584442 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688475 | GGATAAAATGAAGAA[A/C]TGACTCAAAATTGAG | 6468 |
rs6584443 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691868 | CCATTATCATGAATA[A/C]AATCATCCTAGAATA | 6468 |
rs6584444 | snp | C/T | 0.400147 | 0.19989 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696052 | ATTTTAATGTAACTA[C/T]TAGAAAATTTAAAAT | 6468 |
rs7068187 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682560 | AAACTAAAAAGGGAG[C/T]ACTCTGGATCATAGC | 6468 |
rs7071326 | snp | A/G | 0.372391 | 0.217992 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674413 | TAATTTGAAGTGTAA[A/G]TGGGAAGTTTCAAGG | 6468 |
rs7072170 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652867 | GCTCCTAGTTTTCCT[C/T]CTGCCTCTGATTGGA | 6468 |
rs7078354 | snp | C/T | 0.37778 | 0.214877 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648812 | GAAAGTCAGGTTTTC[C/T]GATCAGTATTGTTCC | 6468 |
rs7084405 | snp | G/T | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682521 | CTTCTCTTGAATTAG[G/T]TCTAAAATTAATGAG | 6468 |
rs7087836 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650726 | TCTGCCACCAGCCTC[C/T]AGGGCCGAAGACCCT | 6468 |
rs7090062 | snp | A/G | 0.12932 | 0.218944 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648257 | ACAGGTTGGGAGGAA[A/G]AAAGCAAAAATTCTG | 6468 |
rs7095907 | snp | C/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672663 | AGGTCCTCTGTTTTT[C/G]AGTTCACGCCACATT | 6468 |
rs7478084 | snp | A/C | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637420 | aaaaaaaaaaaaGCC[A/C]CCATGagccaggcat | 6468 |
rs7478123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637605 | cccatctacttggga[A/G]gctgaggcatgagaa | 6468 |
rs7895811 | snp | A/T | 0.398174 | 0.201356 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681398 | cgtctcaaaaaaaaa[A/T]aataataataataat | 6468 |
rs7896681 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668870 | TCTCAGACGTACAGG[A/G]CTATCCCAAGACAGC | 6468 |
rs7898842 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648049 | CAGGTCACCCAATCA[C/T]CAGGGAGGTCCCTGT | 6468 |
rs7904157 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675690 | GATGTTCCCTATCCA[C/T]TGCAACCAATCAACA | 6468 |
rs7911220 | snp | A/G | 0.0107246 | 0.0724382 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695385 | TGCCTGAGGCCACAA[A/G]AGGACCCGCTGCCCT | 6468 |
rs7914471 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648527 | GCAGCAGTGGCAACA[A/G]GAAAAGGAGTCAGAA | 6468 |
rs7916943 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684303 | tactttatttttgta[A/T]ttttagtagagacag | 6468 |
rs9419933 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619590 | cgtgaacccgggagg[C/T]gttaggcaacggctg | 6468 |
rs9651449 | snp | C/T | 0.259674 | 0.249813 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631199 | AAGAGACAGTGCAGA[C/T]AGAAAATTTAAATTC | 6468 |
rs9651450 | snp | C/T | 0.287085 | 0.247234 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632388 | AAAGCAGGGTTTCTG[C/T]GGAGGAGTGCATTCC | 6468 |
rs9651451 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665538 | ATGAGACACATCGAG[A/G]CCTTAGCAGAGGGTC | 6468 |
rs9731161 | snp | A/T | 0.0543475 | 0.155628 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685696 | TGAAACTTGCTTTTT[A/T]AAAAAAAAATGACAT | 6468 |
rs10564210 | in-del | -/ATTT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680062 | TGCACAAAAGTCATT[-/ATTT]CATTCCTTTTTATGG | 6468 |
rs10688145 | in-del | -/AAACA/AACAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641643 | AAAAAAACAAAACAA[-/AAACA/AACAA]TACACATACACCTTA | 6468 |
rs10786640 | snp | A/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632876 | ACAAGAAGCATGCAA[A/T]AAGACAAGCTATACA | 6468 |
rs10786641 | snp | A/G | 0.287606 | 0.247155 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633122 | CATAAGACAGAAATA[A/G]TAATAGTACCTAGGC | 6468 |
rs10786642 | snp | A/G | 0.287606 | 0.247155 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633169 | AATTATATGGGAAGT[A/G]TAAATTAGTTCAACC | 6468 |
rs10786643 | snp | A/G | 0.191775 | 0.243125 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634284 | AACTTTACTAAAGAA[A/G]ATAGAATTGTTGAAT | 6468 |
rs10786644 | snp | C/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636889 | CCACTGCACCCAGCC[C/T]AGGATTACATTTAAA | 6468 |
rs10786645 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659694 | TGAGGTTGTAGTAGA[C/G]TTTCTTCTGAATACA | 6468 |
rs10786646 | snp | A/G | 0.377977 | 0.21476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679345 | TGCCCAATGCCTTAC[A/G]CATATCAGTAAGTGC | 6468 |
rs10883665 | snp | A/G | 0.18325 | 0.240924 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614476 | GAAAATGTCATGGCC[A/G]TAAGTATCTGCAGTC | 6468 |
rs10883666 | snp | G/T | 0.277334 | 0.248501 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615355 | CCCAGGCCTCCAGGA[G/T]CCACTAAGGGCTGGG | 6468 |
rs10883667 | snp | A/T | 0.186737 | 0.241863 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625092 | GCACACCATAAAAAC[A/T]GATCTCTAGACGTGA | 6468 |
rs10883668 | snp | A/G | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639077 | CAAGCCCTGGTGCAC[A/G]TGTCAACTCCCTGCA | 6468 |
rs10883669 | snp | A/G | 0.209997 | 0.246779 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641859 | ATATCACTGTATAGT[A/G]TATCAATAGACACAC | 6468 |
rs10883670 | snp | C/T | 0.254944 | 0.249951 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642127 | GCCGAGACTGTGCCA[C/T]TGCACTCCAGCTTGG | 6468 |
rs10883671 | snp | G/T | 0.174932 | 0.238463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654105 | CAGACCGGCGACAGA[G/T]CGAGACTCCGTCTTA | 6468 |
rs10883673 | snp | C/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664955 | TCATATTTAATATGA[C/T]GAAACTGAGGCTGGG | 6468 |
rs10883674 | snp | A/G | 0.321053 | 0.23969 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665811 | AGCCTAACACATTCC[A/G]GAGGAGGAGGCTGGA | 6468 |
rs10883675 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684009 | CACTGTGTCACCCAG[A/G]CTGGAGTGCAGTAGC | 6468 |
rs10883676 | snp | A/C | 0.175897 | 0.238765 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685568 | CATATATGAACTTTA[A/C]CTCAAAGGATATAAG | 6468 |
rs10883677 | snp | A/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685702 | TTGCTTTTTTAAAAA[A/T]AAATGACATTTACCT | 6468 |
rs11191065 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613500 | TGGACACTTCACAGG[G/T]ATGTCCAGGTAAGAG | 6468 |
rs11191067 | snp | G/T | 0.185788 | 0.241613 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620125 | GGCGCTCCTCAAGTT[G/T]CAGCAGTGACAGGTT | 6468 |
rs11191068 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621511 | ccagcctgggtgaca[A/G]agcaagtccctgtct | 6468 |
rs11191069 | snp | G/T | 0.170733 | 0.237101 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628372 | CTGACCATCCTTCTA[G/T]TCCTTTCCATACTCA | 6468 |
rs11191070 | snp | C/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637105 | AAAGCCACCATGggc[C/T]gggcacggtggctca | 6468 |
rs11191071 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638483 | GACACATACTGGATG[C/T]CCTGCAAAAAAAAAA | 6468 |
rs11191072 | snp | G/T | 0.289683 | 0.24683 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640309 | GCTTGAGGGATGGGA[G/T]TCTAGTCTTCAAGGG | 6468 |
rs11191073 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640818 | accctgcccaaccTA[A/G]ACTCTTCCTTCCCCC | 6468 |
rs11191074 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653161 | CCTGATGTGCAGTCA[C/T]GTCTGACTACTGATT | 6468 |
rs11191075 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654020 | cagctacttgggagg[C/T]tgaggcaggagaatc | 6468 |
rs11191076 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654117 | agagcgagactccgt[C/T]ttaaaaaaaaaaaaa | 6468 |
rs11191077 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654797 | tattttatcagaacc[C/G]tactcatggatattt | 6468 |
rs11191078 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662536 | AGTTTCTACACCTAT[A/C]CCACTCATATATTTC | 6468 |
rs11191079 | snp | A/G | 0.378372 | 0.214524 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663001 | CCTTTTATGGGCCAC[A/G]GCTACCATCCAAGAT | 6468 |
rs11191080 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664690 | CAGACTTGACAGCAG[C/T]TGAAGCCACTAAGCA | 6468 |
rs11191081 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669824 | cagtggcgcaatatc[A/C]gctcactgcaagctc | 6468 |
rs11191082 | snp | C/T | 0 | 0 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676386 | CGGCAGCGCCCCAGT[C/T]TCCAGTTCTGAGACA | 6468 |
rs11191084 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676662 | TGATGCCAAAGCAAT[C/T]TAATGGAGAATGCAT | 6468 |
rs11191085 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676828 | ACTATAAAGCTGTCA[A/G]AAGAAAATATATAAA | 6468 |
rs11191086 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676855 | TAAAAACATCTCTCA[A/G]ACTAAGAAGGTAGAC | 6468 |
rs11191087 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676926 | AAATCCAGTAAATCA[A/G]ACTTCATCAAATCCA | 6468 |
rs11191088 | snp | C/G | 0.176219 | 0.238865 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677509 | TCAGAACAGTCATTA[C/G]TACCAGGATAGGGAT | 6468 |
rs11191089 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684028 | GAGTGCAGTAGCACA[A/G]TCTGGGCTCAACGCA | 6468 |
rs11191090 | snp | C/T | 0.327914 | 0.237549 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684421 | GTGAGCCACTGCGCC[C/T]GGCCTACCCAGCTAA | 6468 |
rs11191091 | snp | A/C | 0.176219 | 0.238865 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688892 | TTTGGAGCCTGGTCT[A/C]AATAAGAATCTGCCT | 6468 |
rs11191092 | snp | C/T | 0.176219 | 0.238865 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689494 | ATTAAAAATAAGGCC[C/T]TTCCAAACGCCGAAG | 6468 |
rs11286397 | in-del | -/T | 0.408359 | 0.193449 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631630 | AAACACATTATTTAC[-/T]TTTTTTTTTTTTTTT | 6468 |
rs11287325 | in-del | -/T | 0.322007 | 0.239405 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642387 | GGGACCCTATCTCTA[-/T]TTTTTTTTTTAATTA | 6468 |
rs11431014 | in-del | -/A/AA/AAAAAAAAAAAA | 0.44306 | 0.158832 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674326 | CAAAAAAAAAAAAAA[-/A/AA/AAAAAAAAAAAA]GAAAGAAAGAAATCT | 6468 |
rs11591384 | snp | A/T | 0.293294 | 0.246223 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693549 | GAGGTGATGGTATTA[A/T]GGCTTTTTATGTTTT | 6468 |
rs11593799 | snp | C/G | 0.0379877 | 0.132479 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635832 | ggcaacagagcaaga[C/G]ccggtctcagaaaaa | 6468 |
rs11594390 | snp | C/T | 0.322959 | 0.239117 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657818 | GATGCATGTATTCTT[C/T]ATTGTCATCATGTGT | 6468 |
rs11815310 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612748 | CGGCTGCCACCCACC[C/T]AGCCACTCCTCCTCA | 6468 |
rs11815874 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674195 | ttagacaggcatagt[A/G]gtacacgccggtaat | 6468 |
rs11817043 | snp | A/G/T | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637608 | atctacttgggaagc[A/G/T]gaggcatgagaattg | 6468 |
rs11818882 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695240 | GCACGCCCCTCACAC[C/T]TGCAGCCTTGGAGCC | 6468 |
rs12240593 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693207 | CTGGTCCCACTATAA[A/T]TTGGTACAGCACCTC | 6468 |
rs12241077 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632012 | GACCTGAAGGTGAGC[A/G]ACCTGGTACAGCTAG | 6468 |
rs12241580 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657095 | CTCCAATCCTCCCGC[C/T]CTTGTCAGCACCTCA | 6468 |
rs12243184 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633293 | ttataaatcattcta[C/T]tataaaggggacatc | 6468 |
rs12244100 | snp | C/T | 0.154661 | 0.231107 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619640 | ctccaccctgggtaa[C/T]agagcaagactctgt | 6468 |
rs12246015 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689352 | ATGGTCTTAGAGAAG[C/G]CTTCTTCCATTCTTC | 6468 |
rs12249989 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691139 | CATCTCACTTATCTA[A/G]TCTGCAGTTAATTAG | 6468 |
rs12255066 | snp | A/G | 0.269809 | 0.249214 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613836 | GAATTAATCCCCAAG[A/G]CAGCACCCCTGCTAC | 6468 |
rs12255638 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662062 | GGGCCAAAGGACTGC[A/G]GCACCACTGGCAACC | 6468 |
rs12255642 | snp | A/G | 0.17332 | 0.23795 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696969 | TTGAGTACTTAACTC[A/G]TTCAGGATACATAGT | 6468 |
rs12255825 | snp | A/C | 0.176219 | 0.238865 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662350 | GGGAGAAATGAAGCA[A/C]GAAGGGGCAGCTCCT | 6468 |
rs12261004 | snp | C/T | 0.186737 | 0.241863 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622706 | gcactccagcctggg[C/T]gacatagtgagactt | 6468 |
rs12261112 | snp | A/C/T | 0.0193847 | 0.0965802 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677026 | gacaggaatttgtaC[A/C/T]GTGATGAGGAAGTCC | 6468 |
rs12262279 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693147 | AATGACCACTAAAGT[A/G]GCAAAGATTTTCTAA | 6468 |
rs12263004 | snp | A/G | 0.0532157 | 0.154195 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683534 | AAGTGAGTCCAGAGG[A/G]ACAGAAATTAATCTA | 6468 |
rs12267059 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625104 | AACAGATCTCTAGAC[A/G]TGACAAGTTTGAGCC | 6468 |
rs12354716 | snp | A/C | 0.186737 | 0.241863 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627018 | CCACCAGGAGGAGTG[A/C]CCCTCACCTTCATAC | 6468 |
rs12356764 | snp | C/T | 0.176219 | 0.238865 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666997 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 6468 |
rs12357137 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673263 | ATATATTTTCCCCTG[A/G]AGAATATCAAAACCA | 6468 |
rs12358045 | snp | C/T | 0.190205 | 0.242744 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639951 | ATTTGGTTTCTGTCA[C/T]TTACAATAAATGTGT | 6468 |
rs12358746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676894 | cttaggacacagaaa[A/G]caataacagaaaata | 6468 |
rs12414932 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641051 | ggccaggctggtgtc[A/G/T]aactcctgacctcag | 6468 |
rs12570717 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632707 | AGGGAGAAGAGTTTC[C/T]AAACTGGATTTCCAT | 6468 |
rs12571063 | snp | A/G | 0.00956916 | 0.0685055 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636923 | tatcactatctttta[A/G]agtacagactgaaat | 6468 |
rs12571662 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644587 | CTCTCTCCAGAGGGC[C/G]TGGGGCTGGAGCTCA | 6468 |
rs12763164 | snp | G/T | 0.0140508 | 0.0826316 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682939 | TTTTGTCTAACCATC[G/T]TGGATGGTTACAGTT | 6468 |
rs12765692 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657279 | GCAGAGGGATTTCGT[C/T]TGAGGCACACAAGCA | 6468 |
rs12769363 | snp | A/C | 0.0200648 | 0.0981316 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662738 | GAGCTGTGGGCGCCT[A/C]TCCCTTCCCCTCCCA | 6468 |
rs12773760 | snp | A/C | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694949 | cttccgccccgcttc[A/C]tcttccgccttgccc | 6468 |
rs12779644 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692284 | atacacacatatatg[G/T]ctatgtgtatataca | 6468 |
rs17114146 | snp | C/T | 0.111576 | 0.20818 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641759 | ATCAGAAATTAGGTA[C/T]GAGGAAACCAAAGCT | 6468 |
rs17114147 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644844 | TCCAGTCATGCCAAC[A/G]AAAATGAGATCATAC | 6468 |
rs17114149 | snp | A/G | 0.0923359 | 0.194016 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646591 | GACTGTGAGGCAGCC[A/G]GGAAGGCCAGGGGAC | 6468 |
rs17114151 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647020 | CATGGCTTCAGTCAG[C/T]GATACCACAAAACTC | 6468 |
rs17114166 | snp | C/T | 0.039522 | 0.134904 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691479 | ACCCTAGGACATGGG[C/T]GAGAAATCAAAACAC | 6468 |
rs17696300 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617239 | AGGCGCAGGGGTCAC[A/G]CACCTAGTAAATCTT | 6468 |
rs17696674 | snp | A/T | 0.124491 | 0.216211 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655306 | CTTTTCCTCTTTTTA[A/T]TCTTGAACTCATCCT | 6468 |
rs28565478 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659949 | TATAATAATAATAAT[A/C]AAAAGGAGGAAGATA | 6468 |
rs28607887 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651343 | AGGGTGGGAAATGGG[G/T]GGGGGGTGAAAGAAG | 6468 |
rs34104336 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611030 | TGCTCTGGCCAAACA[-/G]GGGACGCAAGGCCCG | 6468 |
rs34108114 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675978 | TTGTAAAATAAGATG[-/C]AATTGAAACCTTGAT | 6468 |
rs34174886 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679935 | TTACACCACTCTGTA[A/C]GCCTGTGTGTACCCA | 6468 |
rs34189071 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617104 | AACAGCTCACATATC[C/T]TGAGTCCATACTGTG | 6468 |
rs34252784 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690316 | TCCTCTTACTCTTTA[-/G]GGAAAATTTGAAAGA | 6468 |
rs34301219 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620581 | TGGCCAGAGCGGGCA[-/G]GGGCTGTTTCTTCTC | 6468 |
rs34449188 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675713 | ATCAACAAGGAGCAA[-/T]TTTTTTGGTAGAGAG | 6468 |
rs34463792 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637722 | GCAAGATCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs34484310 | in-del | -/A | 0.0364509 | 0.129988 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634201 | AAGAATAAATCTAAC[-/A]AAAAAAAACAAGAGA | 6468 |
rs34555078 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620375 | CCATTTCCTCCCACC[-/A]AAAAGCAAATGCCTC | 6468 |
rs34560754 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627592 | ACAGACCAGCCACAC[-/T]TCAAAGTCAGAAGAT | 6468 |
rs34795580 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686228 | AGATATTTAGCAGTG[-/A]AAAAAAGAATTTTAT | 6468 |
rs34806581 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639468 | TCACATAGACACTTT[-/G]GGGACTGGACATCAT | 6468 |
rs35007250 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101625806 | ATGTCCCTGCATGTC[-/T]TTTCATGGGGGGGAA | 6468 |
rs35036519 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639639 | ATGCGCAGCTGACCC[-/A]AAAACTGGCCTGGGA | 6468 |
rs35098665 | in-del | -/A | 0.138886 | 0.22395 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689134 | TGCAAAAAAAAAAAA[-/A]TGAAAGTATGGAGTA | 6468 |
rs35099922 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661507 | CCAAATCAATGACAT[-/C]CCCCACACTGATCCC | 6468 |
rs35116530 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687262 | AGAAGAAATATAATA[-/C]CCCCTTCGGACTGCT | 6468 |
rs35146403 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101643832 | TTGTTTCATCCCTAA[-/G]GGGGCCTGGGGTAGG | 6468 |
rs35209506 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611262 | GTAGCTGGTTTCCCT[-/G]GGCCCAGAGGCAGGG | 6468 |
rs35329839 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642780 | ACATCATGAGCCACA[-/G]GGGGAGCACTGGGGC | 6468 |
rs35395921 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101617198 | AGGTAAGTTTCTTAA[-/C]CCCCATTTTACAGAT | 6468 |
rs35424689 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101626926 | GGATGAGGGTGGTGT[-/G]GGGGATGTAAATCCC | 6468 |
rs35508684 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623827 | TAAAAAGCCAGTTTC[-/A]AAAAGTGACATATTG | 6468 |
rs35601713 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627374 | ACACTCAGTAAAAAA[-/C]CCATCAATAGTCAAG | 6468 |
rs35614606 | snp | C/T | 0.0112461 | 0.074139 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612369 | TGGCTATGACACCTA[C/T]GTTCGCTACTGGGAC | 6468 |
rs35660829 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612700 | CCCCCAGCATCCCAG[-/T]CCCTCAGCAGCCCCT | 6468 |
rs35664019 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624092 | CATAGACACAGACAG[-/AC]ACACACACACACACA | 6468 |
rs35721394 | in-del | -/A | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657639 | GCGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs35728166 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101683862 | CTCAGGAAAGGAAAG[-/T]TGTCTCCAAGTGTAC | 6468 |
rs35789744 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101615235 | GCTTGTGTGGGAACA[-/G]GGGCTGCTGCTCAGA | 6468 |
rs35920307 | in-del | -/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616415 | TGTCCCTGCCTTCAA[-/G]GGAGTATTCAATCCA | 6468 |
rs35945536 | in-del | -/A | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696822 | TGATGTCATGAGTTC[-/A]AATATTTATTGATTT | 6468 |
rs55827061 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665915 | CGCACAGACCATCTC[C/T]GGCCCTGAGAGCTTC | 6468 |
rs55828979 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678772 | TATACCGTCACATTT[G/T]CCAAATTTTACTAAA | 6468 |
rs55889686 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640857 | CTTTTTTGAGACCAA[A/G]TCTCACTCTGTCGCT | 6468 |
rs55891130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672457 | CTGCTGCTTACTGAC[C/T]ACATCACTCTCCAGA | 6468 |
rs56053113 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645082 | TGCTCCTTCAATGGC[C/T]TGGGCTGGCTGCTAA | 6468 |
rs56074268 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652074 | ATAAAATTTCTCTCT[C/T]TGATTCCTTCTTTGC | 6468 |
rs56103709 | in-del | -/CA | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624119 | ACACACACACACACA[-/CA]GAGTGCAATCTGAAT | 6468 |
rs56232127 | in-del | -/A/AA/AAA | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676736 | AAAAAAAAAAAAAAA[-/A/AA/AAA]TGAAATGAATCCTGA | 6468 |
rs56308314 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640800 | GGATTACAGGTATGA[A/G]CCACCCTGCCCAACC | 6468 |
rs56866043 | snp | C/T | | | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676394 | CCCCAGTCTCCAGTT[C/T]TGAGACACCTTCACT | 6468 |
rs56970368 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664450 | GCCAGTACACTGGCT[A/G]CCACATCCCCTCATA | 6468 |
rs57078445 | in-del | -/AAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637720 | AAAAAAAAAAAAAAA[-/AAA]GGTCACTATGAGGTT | 6468 |
rs57714649 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101616744 | GGGTCTGGCCTCCAG[C/G]CCACAGTGGGCCTTA | 6468 |
rs57745362 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652611 | GAACTAGAAAAAAAA[-/AA]GGCAAATTTATTATA | 6468 |
rs57915175 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666821 | ATGCACTTTGGGAGG[C/T]CAAGATGGGAGGATC | 6468 |
rs57953088 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641491 | CAAATGACCCAAAAA[A/C]TAAGGGAAAAATAAA | 6468 |
rs59115822 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683561 | TCTAGGCAGTTATCT[A/G]GAATGACCTTTCATT | 6468 |
rs59895769 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101666934 | AGAATGAAAAAAAAA[-/A]CCACCCCATTTCTAG | 6468 |
rs60232353 | snp | A/G | 0.0138799 | 0.0821421 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610253 | ACAGAGCAAGACTCC[A/G]TCTCAAAACAAAACA | 6468 |
rs60239868 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692238 | AACTGTATCAGTGAC[A/G]CACAATGAAGAGTTC | 6468 |
rs60301042 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642316 | AGCACTTTGGGAAGC[C/T]GAGGCAGGAGGATTG | 6468 |
rs60453783 | in-del | -/TAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681759 | TAATAATAATAATAA[-/TAA]CAGGTCTAAAGATGT | 6468 |
rs60568785 | in-del | -/A/AAAA/AAAAA | 0.625 | 0.125 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654139 | AAAAAAAAAAAAAAA[-/A/AAAA/AAAAA]TCCAAAGCTTATATT | 6468 |
rs60654508 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692038 | TGCAACAACAGATAT[A/G]TAAGAACTTTATCAT | 6468 |
rs60780132 | in-del | -/GAG | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101655690 | GGCGGAAAATAGCAG[-/GAG]AAGGAAACACCCTGC | 6468 |
rs60895988 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677799 | CTAAAAAAAAAAAAA[-/A]GAGAAAAGAAATACA | 6468 |
rs60928968 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612791 | GGGGGGCTTGCTGAA[A/G]GGGTCGGCCCCCCTC | 6468 |
rs61272692 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622041 | AGTTTCCCATCCCTG[C/T]TCTTGGATGACTATC | 6468 |
rs61319559 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622750 | AAAAAAAAAAAAAAA[-/A]GACAAGCTACAGATT | 6468 |
rs61382490 | snp | A/T | 0.352926 | 0.227829 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694645 | GCCGCCGCCATGGCC[A/T]CCCCTGTCCCCGCGA | 6468 |
rs61568213 | in-del | -/CA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624120 | ACACACACACACACA[-/CA]GAGTGCAATCTGAAT | 6468 |
rs61631625 | in-del | -/A | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692768 | AAAAAAAAAAAAAAA[-/A]TCAAATTTGTAAGAA | 6468 |
rs61742882 | snp | A/G | 0.00124204 | 0.0248893 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673044 | AATGCCAATCTTCCC[A/G]TCCCTAGGAGAGAAA | 6468 |
rs61748908 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672862 | AGGGATCTATCCACC[C/T]CCTCCCTATAGACAG | 6468 |
rs61761937 | snp | C/G | 0.10382 | 0.202809 | intron-variant, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694572 | GAGCGCAGGCCCCGC[C/G]GCCGGGCGGGCAGCC | 6468 |
rs61874048 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627069 | TTTTTTTTTTTTTAA[A/T]TAGAGACAGGGGTCT | 6468 |
rs61874049 | snp | C/T | 0.155987 | 0.23165 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631918 | AGGCGTGAGCCACCG[C/T]GCCCAGCCATTATTT | 6468 |
rs61874050 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663899 | TTCTTTTCCAGGTCA[C/T]GAATCTTAAAAACAG | 6468 |
rs61876362 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101677893 | TTAAAAAAAAAAACC[A/C]ATAAACTAATATACT | 6468 |
rs66647625 | in-del | -/TTA | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681757 | ACATCTTTAGACCTG[-/TTA]TTATTATTATTATTA | 6468 |
rs66921816 | in-del | -/T | 0.447809 | 0.152878 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669759 | ACTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 6468 |
rs67259257 | in-del | -/ACCACC | 0.375 | 0.216506 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656263 | GATAAGCATGGGGTG[-/ACCACC]ACTTTGATTATGTTG | 6468 |
rs67278931 | in-del | -/TTTCTCTCCTGT | 0.37955 | 0.213815 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675493 | TCATAAAAATCCGTC[-/TTTCTCTCCTGT]AGTTTCTTTACCATC | 6468 |
rs71016336 | in-del | -/T/TT | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657663 | TTTCAGATAGTGAGC[-/T/TT]TTTTTTTTTTTTTTT | 6468 |
rs71472583 | in-del | -/A | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634209 | ATCTAACAAAAAAAA[-/A]CAAGAGAAAAATGAA | 6468 |
rs71871812 | in-del | -/AAAA/AAAAA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654136 | AAAAAAAAAAAAAAA[-/AAAA/AAAAA]AAAATCCAAAGCTTA | 6468 |
rs72844617 | snp | C/T | 0.108048 | 0.20579 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612681 | CAGTCCCAGGCCCCA[C/T]CCCTCCCCCAGCATC | 6468 |
rs72844618 | snp | C/T | 0.107694 | 0.205546 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629578 | CATGAGCCACCGCAC[C/T]CAGCCCCACTTTCCC | 6468 |
rs72844622 | snp | A/G | 0.0498117 | 0.149749 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646279 | ATTTAACCTGGCCAG[A/G]GCCTCAGGAGATTCT | 6468 |
rs72844629 | snp | C/T | 0.110872 | 0.20771 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663600 | AGTTCAAGTGATATA[C/T]AATTGTGCCACTGCA | 6468 |
rs72844630 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666684 | GTCTATGTACTCTGC[C/T]GGGGAGGAGAGGGAT | 6468 |
rs72844632 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689809 | TCTCACCACTCTGGA[C/T]GTTAATCATCACTGA | 6468 |
rs72844633 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691074 | CCTAGGGCCAGTGAG[A/G]TTATGTGGCTTCTGG | 6468 |
rs73336840 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695344 | GGAGTTCGCGCTGCA[A/G]ACACGTGAGGCCGGT | 6468 |
rs73336841 | snp | C/G | 0.0524604 | 0.153226 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695353 | GCTGCAAACACGTGA[C/G]GCCGGTTTCAGGGCC | 6468 |
rs73336844 | snp | A/G | 0.0524604 | 0.153226 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695449 | GAAGCCCCTAGTTGG[A/G]TGGCCTTGCCCCTCT | 6468 |
rs73349895 | snp | C/G | 0.0242184 | 0.107344 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611284 | GAGGCAGGGGTGGCC[C/G]TGACGGTCATGGGTT | 6468 |
rs73351212 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648130 | GAAGAAGATATCCTG[C/T]GATTTGGGTTTTTTT | 6468 |
rs73351217 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653726 | TACATGCATTGTTTC[C/T]GCAATTGCACTATAA | 6468 |
rs73351221 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655396 | TTGAATAATTTGTGG[G/T]TTTTTTTCCTATTAA | 6468 |
rs73351236 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665720 | ATGCTTCTTAATGAT[A/G]AGGGCAGACTCTGTC | 6468 |
rs73351242 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666740 | AAAGCAGAAGTCGGG[A/T]TGCAAACCTCACTTG | 6468 |
rs73351264 | snp | A/C | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677261 | ATAGCCAAAAGTGGT[A/C]AACAGCCCAGGCATC | 6468 |
rs73351267 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677839 | ACACAAGATTTGTGC[A/G]GTTTACTCAAATATA | 6468 |
rs73351268 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678011 | ATACAGCCAAATATT[A/G]ATTGTAGAACCTAGG | 6468 |
rs73351271 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678545 | ACTCTCCTGCCTCAG[C/T]CTCCTAAGAAGCTGG | 6468 |
rs73351274 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678587 | CCCACCACCACACCC[A/G]GCTAATTTTTTTTAC | 6468 |
rs73351280 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686330 | GCCTTTAATCCCCAA[C/T]GGACATTGTGATCCC | 6468 |
rs73351283 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688442 | CCAGACTTCCAGGGA[A/G]GGCAATGTGGACAGT | 6468 |
rs74153049 | snp | C/G | 0.128632 | 0.218563 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665248 | CATCTAGTGTAAAGA[C/G]AGAATCTCAAACACA | 6468 |
rs74153052 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688023 | GGTTGAGTGAAGACC[A/G]TGAAAACTGTACAAG | 6468 |
rs74153057 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695564 | CAGGTTCCATAGCTT[A/G]GGTTCTCACACAGGC | 6468 |
rs74233238 | snp | A/C | 0.093777 | 0.195178 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634832 | TAATCTTGGAAAGAC[A/C]TTCTTAAGATAAACA | 6468 |
rs74430890 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643392 | CCTAGTCACAGCCTT[A/G]GGAAGAGGTACATGC | 6468 |
rs74681050 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624522 | TTGTTGTTGTTATCA[G/T]AAATTCTACATGAAA | 6468 |
rs74770417 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651014 | TCGGCAGCCTTTTCA[C/T]GGGGAAGATGCCTCT | 6468 |
rs74806890 | in-del | -/C | 0.283421 | 0.247756 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615045 | CCCTCCTCCTGGGCT[-/C]CTTTTCTTACTGCAA | 6468 |
rs74926559 | snp | A/G | 0.173965 | 0.238157 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618552 | GAGGTGGAAGTGGAG[A/G]TGTAACATGGGACCA | 6468 |
rs74958458 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664401 | AACAAAGGGTTGAGA[A/G]ATTGGCAGGTAAACC | 6468 |
rs75046922 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692439 | GCACCAAAAGTGATA[C/T]TGATGAAAGTGTTAA | 6468 |
rs75079636 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637487 | CCAAGGCGGGCAGAT[C/T]ACTTGAGGCTAGGAG | 6468 |
rs75159925 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637564 | AATACAAAAATTAGC[C/T]AGGTGTGGTGGTGCA | 6468 |
rs75170430 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635857 | GAAAAAAAAAAAAAA[A/G]GAGAGATGGAGGGGC | 6468 |
rs75225896 | snp | C/T | 0.030278 | 0.119257 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683640 | TAGTCTGAAGAAAAC[C/T]GGCTGGGGGGAAGGA | 6468 |
rs75299772 | snp | A/G | 0.174932 | 0.238463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659230 | CCCTCACTCCCCTTC[A/G]GCAAGACCCCAGGGC | 6468 |
rs75335005 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644189 | TTTCCAGTGAATGGT[A/G]GGGAAACTTTGGCAT | 6468 |
rs75417465 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629303 | TCCCTTTTTTTTTTT[G/T]AGACAGAGTCTTGCT | 6468 |
rs75454639 | in-del | -/A | 0.191461 | 0.24305 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618893 | AATGCCCCTTGGCAG[-/A]AAAAAAAAACCCACA | 6468 |
rs75470108 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616372 | GAAACTACAGGGAGA[C/T]GTAAGCTGTGACTTG | 6468 |
rs75507119 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615392 | CACACCCTAGCCTCC[A/G]CCGAGTCAAGTCCAG | 6468 |
rs75582201 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613045 | GAGAAAGCAGCTTAG[C/T]GAGCTGTCCCTGGTG | 6468 |
rs75671305 | snp | C/T | 0.111224 | 0.207945 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640193 | GAGATGAGGTGTTCT[C/T]TTATACCAATGCCTA | 6468 |
rs75702040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628839 | GACTCCATAAGCTCT[C/T]TTTGGAACAGAAAGC | 6468 |
rs75722972 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668364 | CATCTCTCACCAAGA[C/T]TTTACTTTGGAGAAG | 6468 |
rs75811036 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627199 | CTCAGCCTCCTGTGA[A/C]GTGCTTTCTTAACTG | 6468 |
rs75842902 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622450 | AAAAGACAAGCAGCC[A/G]GGTGCGGTGGCTCAC | 6468 |
rs75972556 | snp | A/G | 0.164873 | 0.23506 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617265 | ATCTTAGATCTATAT[A/G]CTTCAGGGTGGTGGC | 6468 |
rs75973994 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620268 | TCAAACTTTGTCCTG[A/C]CTGTTCATTACCTTA | 6468 |
rs75987871 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621679 | TTGTTCATACCAGTT[A/C]TGTTAGGTAGGGATA | 6468 |
rs76086616 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689542 | ATTCGAAATCATTCC[A/G]TGAATTACAGAACAA | 6468 |
rs76197608 | snp | C/T | 0.126564 | 0.217402 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633139 | AATAGTACCTAGGCA[C/T]TGGCTTGTTATAAAA | 6468 |
rs76281435 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637514 | GGAGTTCAAGACCAG[C/T]GTGGCCAACATGGTG | 6468 |
rs76420628 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620172 | TCCAGCACCGCTCAC[C/T]GCCCAACCCCAAGTC | 6468 |
rs76464262 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691669 | TCATTCATTCACTCA[A/G]TCTCTATATGAAGAG | 6468 |
rs76485911 | snp | A/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631069 | ACAACTTTTTTTTTT[A/T]ATCAAACTAAAGCCG | 6468 |
rs76575159 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682850 | TTTGAAAAAAAAAAA[-/AA]GTTCAATTTGGCTTT | 6468 |
rs76593257 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665035 | AACTCATCTCCCAGA[C/T]TGCTTTAAAGAACAG | 6468 |
rs76611419 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639763 | AGAAAGGAAGGAGCT[A/T]AGAACCATAAAGAAA | 6468 |
rs76613904 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693854 | CCTATATGAAGTCAT[A/C]AACTATGGCTGAACA | 6468 |
rs76636460 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696634 | CAACAAAGACTTTGT[A/G]TAGAAAACGATTTCC | 6468 |
rs76641572 | snp | A/C | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641636 | GATTTTTTCTCAAAA[A/C]AAAACAAAACAATAC | 6468 |
rs76657851 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651327 | GGCCAGTGGGGTGGA[A/G]AGGGTGGGAAATGGG | 6468 |
rs76698826 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677501 | TGAAAAAATCAGAAC[A/G]GTCATTACTACCAGG | 6468 |
rs76794469 | snp | C/T | 0.12932 | 0.218944 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657821 | GCATGTATTCTTTAT[C/T]GTCATCATGTGTAAA | 6468 |
rs76887760 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638503 | CAAAAAAAAAAAAAA[A/G]AGAGTAGGATAACGG | 6468 |
rs76897946 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637515 | GAGTTCAAGACCAGT[G/T]TGGCCAACATGGTGA | 6468 |
rs76978229 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675831 | TTATACTTGCTCTAA[G/T]CTCTAACTCCTGTAA | 6468 |
rs77045412 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631235 | CTTAGCCAACTTCAC[A/G]GATGACTGAACCATA | 6468 |
rs77097749 | in-del | -/C | 0.165527 | 0.235296 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641874 | ATATCAATAGACACA[-/C]ATGTGGCCAGGCACA | 6468 |
rs77183134 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637483 | GAGACCAAGGCGGGC[A/G]GATCACTTGAGGCTA | 6468 |
rs77247384 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632701 | AGCTGCAGGGAGAAG[A/G]GTTTCTAAACTGGAT | 6468 |
rs77290239 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676969 | ACCAAAATGAATACA[A/C]AAGCCGTCGTCTGGG | 6468 |
rs77449307 | snp | A/C | 0.12932 | 0.218944 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625842 | ACTGGACATACTAAT[A/C]ACACATTAGCAATGT | 6468 |
rs77512867 | in-del | -/TT | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642396 | TCTCTATTTTTTTTT[-/TT]AATTAAAAAAAAAAC | 6468 |
rs77582698 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657664 | AAAAAAAAAAAAAAA[A/G]CTCACTATCTGAAAC | 6468 |
rs77625076 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665846 | AGAAATGTTGGGTAG[A/G]GATGCAGGGCAGAGC | 6468 |
rs77656315 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101686011 | GAAGAAATCTGAGCA[C/G]ATAAAGTATCTTAAC | 6468 |
rs77744666 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635662 | CAACAAAGTAAGACC[A/C]TGTCTTTACAAAATA | 6468 |
rs77807983 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644312 | GGCAGCTGGGACTGG[A/G]GCCTGGGCAAGGGAA | 6468 |
rs77893531 | snp | C/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637495 | GGCAGATCACTTGAG[C/G]CTAGGAGTTCAAGAC | 6468 |
rs77896978 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631646 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTCGCT | 6468 |
rs77911865 | snp | G/T | 0.0919752 | 0.193722 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646162 | CCTATACTGTTCCCC[G/T]GCAGTATGGGGTAAG | 6468 |
rs77979640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650878 | GGAGCACACATCGGA[C/T]ACAAAGATCGGGCTC | 6468 |
rs77990860 | snp | C/T | 0.0524604 | 0.153226 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694890 | CGCTCCCGCGTCAGC[C/T]CCCGGCCCGGCTGCC | 6468 |
rs78043220 | snp | A/C | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638488 | ATACTGGATGTCCTG[A/C]AAAAAAAAAAAAAAA | 6468 |
rs78188705 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622749 | AAAAAAAAAAAAAAA[A/G]AGACAAGCTACAGAT | 6468 |
rs78456456 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651189 | GCCACCTGGTCCTTC[C/G]CCCCAGGCCCCAGCT | 6468 |
rs78646802 | snp | A/G | 0.137527 | 0.223271 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632272 | AGGGCAGGATGGTGC[A/G]AGTAGGTGCCTAGGT | 6468 |
rs78718427 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637482 | GGAGACCAAGGCGGG[C/T]AGATCACTTGAGGCT | 6468 |
rs78749696 | snp | A/C | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637478 | TTTGGGAGACCAAGG[A/C]GGGCAGATCACTTGA | 6468 |
rs78779213 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637538 | CATGGTGAAACCCCA[C/T]CTCTACTAAAAATAC | 6468 |
rs78779778 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671279 | AGCTGCAAACCAGCT[C/G]ACCAGCTTGCAGGAC | 6468 |
rs78790917 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682927 | CTTTTTCATATCTTT[C/T]GTCTAACCATCTTGG | 6468 |
rs78797621 | snp | A/G | 0.127944 | 0.218179 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639357 | CTGACTAGTAATAAT[A/G]TGAGGGGGAGGAGGT | 6468 |
rs78831546 | snp | A/G | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637558 | ACTAAAAATACAAAA[A/G]TTAGCCAGGTGTGGT | 6468 |
rs78867302 | snp | A/C | 0.119978 | 0.213528 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674412 | TTAATTTGAAGTGTA[A/C]GTGGGAAGTTTCAAG | 6468 |
rs78913211 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682565 | AAAAAGGGAGTACTC[C/T]GGATCATAGCAGGAA | 6468 |
rs78924389 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662210 | CTGAATATGCATCTA[C/G]CACACACACAACACA | 6468 |
rs79084338 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647911 | ATCCCACCCCCAATA[C/T]TCTGCTATCCCTCTG | 6468 |
rs79134864 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615193 | TGTGGGGGGCGAGAG[C/G]GGGGTGCAGAGCCTT | 6468 |
rs79146152 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662061 | AGGGCCAAAGGACTG[C/T]AGCACCACTGGCAAC | 6468 |
rs79237385 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645580 | GGGCAATCCCTGAGC[A/G]GGGAACAGACAAAGA | 6468 |
rs79328718 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674456 | CATACATACCTCTTC[A/C/T]GCAATAGATCAGTTA | 6468 |
rs79371423 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101654834 | TCTTTTGGTTTTGTT[A/G]CTTTTTTGAGACAGA | 6468 |
rs79467160 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629302 | TTCCCTTTTTTTTTT[G/T]GAGACAGAGTCTTGC | 6468 |
rs79556006 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659424 | AAACTCTCAGCCTCT[A/G]AACAGAAAGAGAGAA | 6468 |
rs79751867 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618933 | AGCCCATGGAGGAAG[C/G]GGGTATTTGTGATGT | 6468 |
rs79758886 | snp | A/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627066 | TTTTTTTTTTTTTTT[A/T]AAATAGAGACAGGGG | 6468 |
rs79856734 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101671129 | GTTATAAAAGACAAA[A/C]TGAATACAATAGTAA | 6468 |
rs79857000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661194 | TTTCATGTAAGTCGG[C/T]TCTTGACAAGTGGGC | 6468 |
rs79877466 | snp | C/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667022 | GGATCACGAGGTCAG[C/G]TGATCGAGACCATCC | 6468 |
rs79878572 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637488 | CAAGGCGGGCAGATC[A/G]CTTGAGGCTAGGAGT | 6468 |
rs80048731 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637435 | ACCATGAGCCAGGCA[C/T]AGTGGCTCATGCCTG | 6468 |
rs80070738 | snp | C/T | 0.0368353 | 0.130617 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696748 | TTATAAAGAAATTTA[C/T]TTATTCACAGGTACC | 6468 |
rs80071787 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617720 | AGGATACAAAATTTC[A/G]ACATCTGTTGCCATA | 6468 |
rs80085258 | snp | A/G | 0.029116 | 0.117091 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611032 | GCTCTGGCCAAACAG[A/G]GACGCAAGGCCCGGG | 6468 |
rs80096562 | snp | G/T | 0.093417 | 0.194889 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635561 | GATGGGAGGCCAGAA[G/T]TGGTGGCTCATGCCT | 6468 |
rs80131409 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666418 | CGGCTCTAATTCTTA[A/G]AAAGAAAAAAAATTG | 6468 |
rs80182750 | snp | G/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692097 | CAGAATTTTTTTTTT[G/T]GACAGAGAGTTGAAC | 6468 |
rs80229203 | in-del | -/G | 0.191775 | 0.243125 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635023 | GCCTGTTAGCAACCA[-/G]GACGCACAGTAGGAG | 6468 |
rs80230537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678154 | CAGCAATAAGAGAAG[A/G]GAGCACACAAGCTAC | 6468 |
rs111250085 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667462 | TGTAAGGGATACTCC[A/G]GAGGACATTTTCCAA | 6468 |
rs111270990 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678672 | TGACCTCGTGATCCA[C/T]CCACCTCAGCCTCCC | 6468 |
rs111418802 | in-del | -/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690620 | TCACAAGGAACCAAA[-/G]CAGTTCATCTTACTC | 6468 |
rs111509520 | in-del | -/AGTA | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667638 | GTTATATTCTCATAT[-/AGTA]AGTACTCTTTCCTTA | 6468 |
rs111600818 | snp | C/G | 0.0462398 | 0.144851 | intron-variant, missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694634 | CCTCCCCGGCCGCCG[C/G]CGCCATGGCCACCCC | 6468 |
rs111774880 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665334 | TTAAAAACTGTTGGT[C/T]AGGAGCTGACAGAGT | 6468 |
rs111776558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674205 | ATAGTGGTACACGCC[A/G]GTAATCCCAGCTACT | 6468 |
rs111831450 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675505 | GTCTTTCTCTCCTGT[A/G]GTTTCTTTACCATCA | 6468 |
rs111947433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664951 | GTATTCATATTTAAT[A/G]TGACGAAACTGAGGC | 6468 |
rs112175038 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613362 | TGGGTGCAAGTATGG[A/G]GTTTCCACAGAATGA | 6468 |
rs112179487 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625568 | AAAACCTCAACATAT[A/G]CAATCTGCAGAGTCT | 6468 |
rs112372206 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674286 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 6468 |
rs112387162 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612877 | ATCCTGCAGGTCATG[C/T]AGTTCTGAGCTGCCT | 6468 |
rs112391054 | snp | C/T | 0.0869089 | 0.189476 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630840 | AAAACAGGCAAATCT[C/T]GTTATCTGTCCAGCA | 6468 |
rs112539111 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630918 | GAGCGCAGCTCCAGA[A/G]GCTGCTCGAGTCACA | 6468 |
rs112575979 | snp | C/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661629 | TCTAGCCATGCCAGC[C/T]CTGGGCCCTCCATGG | 6468 |
rs112621949 | snp | C/T | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652926 | CACTGTCTTTATTTC[C/T]GAATTGTCCTTTGGT | 6468 |
rs112850688 | snp | A/C | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664179 | GTCGTGAGGACCTCA[A/C]ATTAAGCCTCTGGAT | 6468 |
rs112902271 | in-del | -/A | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622752 | AAAAAAAAAAAAAAG[-/A]CAAGCTACAGATTGG | 6468 |
rs112974139 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614745 | TCAAGGCTCTGTTGT[A/G]TGGTGCCCGTGAGGT | 6468 |
rs112991749 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646641 | CGGCCAGCCCTTTTG[A/G]CACCAGCTTCCTTCT | 6468 |
rs113021747 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684382 | CCACCCGCCTTAGCC[C/T]CCCAAAGTGCTGGGA | 6468 |
rs113293672 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682152 | GTCACTAATGTGACT[C/T]TAATAATCATTCGTT | 6468 |
rs113341038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656698 | GCTGTGGGAAGGAGC[A/G]GAGGAAGAGGCAGCA | 6468 |
rs113435727 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653294 | TCTCTCTCCTCCAAA[G/T]AATCCTATATGCTGT | 6468 |
rs113479236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629858 | AATGAATGGACAAAT[A/G]AACAAATGACTCCAC | 6468 |
rs113520095 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101684376 | TGTGATCCACCCGCC[C/T]TAGCCTCCCAAAGTG | 6468 |
rs113778589 | snp | G/T | 0 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619824 | GAACAGTCTCTAGTG[G/T]TCTTGATGGAATGAG | 6468 |
rs113930357 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676712 | GATGTCCAGATTGGG[A/G]AAAAAAAAAAAAAAA | 6468 |
rs113934090 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610980 | TGTCATGGCTCTAAT[A/C]AGGGGTATAGGATGG | 6468 |
rs113961773 | snp | A/G | 0.5 | 0 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666998 | GCACTTTGGGAGGCC[A/G]AGGCAGGCGGATCAC | 6468 |
rs114168325 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646002 | GGGGGGATTAAATAA[A/G]GTATAAAGTGGTCAG | 6468 |
rs114170668 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679980 | CTTATAAGTGAGAAC[A/G]TGTAGTATTTGGTTT | 6468 |
rs114260478 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632267 | GCATCAGGGCAGGAT[A/G]GTGCAAGTAGGTGCC | 6468 |
rs114280213 | snp | A/G | 0.128632 | 0.218563 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636681 | CAACCTCTGCCTCCC[A/G]GAATCAAGCAATTCT | 6468 |
rs114379846 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617496 | CAATGGAGGAGCTAT[A/G]GAAGCTTCACTTGCC | 6468 |
rs114707998 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639491 | GACATCATGGAGTCA[C/T]TTGGCCTTTATCCAA | 6468 |
rs114870461 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666404 | ATGACGTGGCTAATC[A/G]GCTCTAATTCTTAGA | 6468 |
rs114922331 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691495 | GAGAAATCAAAACAC[A/T]CATGTCTAATAAATA | 6468 |
rs115003883 | snp | C/G/T | 0.0123036 | 0.0774623 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655045 | CTGTTGCCCAAGCTG[C/G/T]TCTTGAGCTCTTGGG | 6468 |
rs115155647 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663464 | GCTGGAAATAATTTT[C/T]AAATGGCAATAAAAC | 6468 |
rs115159084 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685420 | ACCATCAAATTTTAA[A/G]CAATATATAGAATTT | 6468 |
rs115289523 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618907 | GAAAAAAAAAACCCA[C/T]AGCAAGAGGAAGCCC | 6468 |
rs115290522 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647975 | ACTTGCTCGGAATCT[A/G]CAGGGAGGGAGATAA | 6468 |
rs115327908 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639915 | TGAGCCAAATATTCT[A/G]TTTTATTTATGTGAA | 6468 |
rs115414728 | snp | C/G | 0.12932 | 0.218944 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658281 | GCCGGGCATGGTGGC[C/G]CACATCTATAATCCC | 6468 |
rs115603008 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643564 | CTAAGGAGCAGATAG[A/C]GGTCTGTGGGCACAC | 6468 |
rs115680910 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662618 | GCCTTCCTGACCACA[C/T]TCTCTCACACGATAG | 6468 |
rs115683381 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669729 | AATTCAAAACAGATC[C/T]ATCCCTGGAAAAGAT | 6468 |
rs115878498 | snp | A/G | 0.124837 | 0.216412 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687510 | TGAAGCTTCTGTACA[A/G]TAACCACCACTCTAT | 6468 |
rs115888755 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626189 | CCTAGCTTCTTCAAG[G/T]CTGCCAGCAGCCACT | 6468 |
rs115971410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641760 | TCAGAAATTAGGTAC[A/G]AGGAAACCAAAGCTT | 6468 |
rs115995973 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652133 | CACTCCGCCCTCCTC[A/G]CCACCAGCTTCAAAC | 6468 |
rs116000963 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667540 | TGTCACCTCCGAGAG[A/G]TGGTGAGAGGCCTCT | 6468 |
rs116067409 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632295 | GCCTAGGTCAGGCTC[C/T]GGATAGTGTCCAGAG | 6468 |
rs116070021 | snp | C/T | 0.00229357 | 0.0337865 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694649 | CCGCCATGGCCACCC[C/T]TGTCCCCGCGATGTC | 6468 |
rs116077462 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642883 | AGGGCAGGGCTGGGC[A/G]TGATGCCTACACTAC | 6468 |
rs116144799 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685936 | TTAAAATGTGTAACA[C/T]ACCACATCTTCAAGA | 6468 |
rs116154802 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644964 | TGTAGGAGCAGTTTG[C/G]CACATGGTTTGTAGG | 6468 |
rs116332253 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658268 | AAAATGGTTTGAGGC[C/T]GGGCATGGTGGCGCA | 6468 |
rs116359176 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678763 | GCCTCTACTTATACC[A/G]TCACATTTGCCAAAT | 6468 |
rs116449345 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690465 | TCTTTGTGTCCCTTT[A/G]AAAAAAAAAGAAAAG | 6468 |
rs116908113 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685900 | ACTTTGAACAACACC[C/T]GTAGCTCCAAAGGCC | 6468 |
rs117124546 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630210 | AGATACAAAGGCAGC[C/T]GAGGAAGGCTTTTTA | 6468 |
rs117272332 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692417 | TAGTAAGTTGAATTC[A/G]CCTCTTGCACCAAAA | 6468 |
rs117281751 | snp | G/T | 0.031825 | 0.122064 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634883 | GGTAGTGATCAGACA[G/T]ACCTAACCTACAAAT | 6468 |
rs117574349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650540 | AAGCTGGCAGCCCTA[C/T]GGGGTAGAACTAACC | 6468 |
rs117644376 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636469 | ACACACATAGTATTT[A/G]ATGTGTGCCCAAGTG | 6468 |
rs117664315 | snp | G/T | 0.0347114 | 0.127086 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694666 | GTCCCCGCGATGTCG[G/T]CCCAAGCCTGACCCC | 6468 |
rs117737803 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634424 | CTTAATCAATTGATT[A/C]TAAAATTCATCTAGA | 6468 |
rs117762261 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689281 | GCTAGAAAATTCAGC[A/C]CCTACCATTCAAGTT | 6468 |
rs117847363 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648227 | CTAAGCATAGACTTG[C/T]AGTGAAAGCAAAGGA | 6468 |
rs117868339 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684764 | TGAATCTTCCAATAG[C/T]TTCAGTAGCAGAGGT | 6468 |
rs117928673 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621477 | AGGCTGCGGTGAGCC[A/G]TGATGATGCCACTGC | 6468 |
rs117980342 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643471 | ACACATACATGCAGC[A/C]GCGTTTGCTCCCTTC | 6468 |
rs118079769 | snp | A/G | 0.030278 | 0.119257 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658568 | GGGGGAATGGTTTGA[A/G]ATGAAAAAGAAAATG | 6468 |
rs118089211 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643420 | TGCCCTCTGGGTTGT[C/G]CTGACCTTGCCATCC | 6468 |
rs118157710 | snp | A/T | 0.130118 | 0.219732 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635446 | CGAGGCTATGGAAAA[A/T]TTGAAAACTGTCTTC | 6468 |
rs137874495 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676133 | TATAATCATAAAAAA[A/G]GTCATTTGTTAAAGT | 6468 |
rs137888238 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611044 | CAGGGACGCAAGGCC[C/T]GGGTTCAGCCGCACT | 6468 |
rs137976296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657041 | ATTCCCTTTGCAATT[A/G]CCATGGCTTCTGCAT | 6468 |
rs138083006 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648330 | GAGATTTTCTACCCC[C/G]TGCTCTTGGGTATAA | 6468 |
rs138185908 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634418 | TTTTTACTTAATCAA[C/T]TGATTCTAAAATTCA | 6468 |
rs138222419 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655791 | AAGGGCCATGATGCC[A/G]TAAGTCTGGGATGAG | 6468 |
rs138269434 | snp | C/G/T | 3.29598e-05 | 0.00405941 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673633 | AATTAGCCTGGGATA[C/G/T]GTACAGAGAATCATC | 6468 |
rs138361408 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618356 | AAGGAGAGCTTCGTG[A/G]TGGAGGTGCTGTTTA | 6468 |
rs138455538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627627 | AAGGGCGTGCGCACA[C/T]GCAATCTCAGGGTAC | 6468 |
rs138484361 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632126 | ATCAGAAGGGAGGTG[C/T]CCCACTGGCCTCTTT | 6468 |
rs138499115 | in-del | -/ATTTAAGAG | 0.0524604 | 0.153226 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641165 | ACCATAATGCCAGGC[-/ATTTAAGAG]ATAGATAATTTAAAT | 6468 |
rs138505099 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662878 | TGGTGCAAGCATTCA[A/C]AGCTACCTGAGTGAG | 6468 |
rs138541181 | in-del | -/A | 0.0520825 | 0.152737 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685695 | TGAAACTTGCTTTTT[-/A]TAAAAAAAAATGACA | 6468 |
rs138555637 | in-del | -/CAGTGA | 0.0283406 | 0.115616 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620128 | CTCCTCAAGTTGCAG[-/CAGTGA]CAGTGACAGGTTAAA | 6468 |
rs138582986 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668923 | AGCCAGATGGATCAG[G/T]GACCTCTTAAGGTCC | 6468 |
rs138668198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642590 | CTCCCCTCCATCCTC[C/T]TGCTCAGGACTTTGT | 6468 |
rs138797501 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101656714 | GAGGAAGAGGCAGCA[A/G]GGCAAGCTAAGCAGG | 6468 |
rs138834469 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661594 | AGCTTCCATCTTTCT[C/G]CGGGTGTCATGACGC | 6468 |
rs139179531 | snp | C/T | 0.124837 | 0.216412 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658501 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 6468 |
rs139209073 | in-del | -/A | 0.0170251 | 0.090679 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696280 | TAAAAATTGACCCTG[-/A]AAATTATTCAACACC | 6468 |
rs139215716 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685169 | TTCATCCATTCTTTA[A/C]AATCTAGATAAAGCC | 6468 |
rs139232571 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679425 | CAATTGGAAATAAGC[A/G]ATAAGCAACTGTCTT | 6468 |
rs139260692 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691376 | AACACGCATAACTTC[C/T]TCCCTCAATCCAGAA | 6468 |
rs139333316 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670956 | ACCCCATAAAATAAA[C/T]CTCTTTCCTAAAATA | 6468 |
rs139341000 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696394 | GAATCTGGCTTTGCC[C/G/T]TAGAATTACTTTTTG | 6468 |
rs139380945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626053 | CAAACCACTGATTTA[C/T]AATAAAAATTGCAGG | 6468 |
rs139406458 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624049 | TATCTGAATCTACAC[A/G]TGATACAATTGCAAA | 6468 |
rs139445072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629429 | GCTGAGTTAACAGGT[A/G]CGCACCACCACGCCT | 6468 |
rs139518859 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622128 | GTTTTAAAAATTTTG[-/A]AAAGACTGACTATAG | 6468 |
rs139543545 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630079 | CAAGTGTATTCAGTT[A/C]TCTTCAACCCGCATT | 6468 |
rs139755607 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652751 | CAGAATAGGGAAAAG[C/G/T]CATAATAAGCAAGGC | 6468 |
rs139768216 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657331 | GAAATAAAACGCCTA[A/C]TTCCAAAAGCTCACT | 6468 |
rs139950803 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101652221 | TAGTTATATCTCTTT[-/A]AAAAAAAAAAAGTTT | 6468 |
rs139976305 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615365 | CAGGATCCACTAAGG[G/T]CTGGGGGCCTCCACA | 6468 |
rs139980926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690506 | ATATCTATTAGTGTT[A/C]ACTGTTCGGGCAAGA | 6468 |
rs140001507 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644953 | TGGCCATGGGCTGTA[A/G]GAGCAGTTTGGCACA | 6468 |
rs140018569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620495 | TCCCAGTGGATGAAC[C/G]TGGGGCTGGAGAGAA | 6468 |
rs140049705 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625491 | AATAACAAACAACGC[C/G]GAGAGGCACACGAGA | 6468 |
rs140109926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658361 | ACCAGCCTGCCCAAC[A/G]TGGTGAAACCCCGTC | 6468 |
rs140181233 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663587 | ACTTGAACCCAATAG[C/T]TCAAGTGATATATAA | 6468 |
rs140255078 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638322 | GAAAGGACCTCCAAG[C/T]CTCGTAGGGAGATGA | 6468 |
rs140281287 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675731 | TTTTGGTAGAGAGTC[A/C]AATAATAACTATGAA | 6468 |
rs140286143 | snp | A/G | 0.000115381 | 0.00759455 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611663 | GCCGGTCCCACAGCC[A/G]TACAACACCGTAGTA | 6468 |
rs140301627 | snp | A/G | 0.0644693 | 0.167566 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610173 | TGAGGCAGGAGAATC[A/G]CTTCAACCTGGGAGG | 6468 |
rs140320532 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616130 | CTACCTGTGCACCTG[A/T]CTGCCATGTGCTACC | 6468 |
rs140378069 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666344 | TCTCCGGGGTCAGCA[A/G]TGTGTTTCAGGTCCT | 6468 |
rs140399994 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644032 | AATTATTCCCCCCAT[C/T]CCACATTCGTACCTG | 6468 |
rs140435140 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650335 | TCTGCCTCTTTTCTG[C/T]CTGGTCTCTATTCTC | 6468 |
rs140487661 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659812 | CACATATCCATGTTA[C/G]AATACACTTTTTAGG | 6468 |
rs140509469 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640031 | ACTGAATGTCCTCAC[G/T]GAGAGATGAGCAAAG | 6468 |
rs140668651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665838 | TGGAATAGAGAAATG[C/T]TGGGTAGGGATGCAG | 6468 |
rs140743763 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683232 | CATATGGTTACTAAT[A/G]TAAAGTGAGGGTGCT | 6468 |
rs140812056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671794 | TATGAAGTAGGGTAA[C/T]AGGAAGCAAGTGACA | 6468 |
rs140851729 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674852 | AAAGAAGACTGTCAG[A/C]TACTAGGCTCTCTGG | 6468 |
rs140880998 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617238 | AAGGCGCAGGGGTCA[C/T]GCACCTAGTAAATCT | 6468 |
rs140884340 | in-del | -/TT | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661741 | GACACCAAGCCACTC[-/TT]TGACTAGCTCTTCAG | 6468 |
rs140917838 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625026 | TGGCCAGAAGACCCA[C/T]GAGCTCAGCCACAGC | 6468 |
rs141066621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632457 | TATTCTCTATTTTAA[C/T]GAAGGGTACAAGGTC | 6468 |
rs141202852 | snp | C/G | 1.64765e-05 | 0.00287019 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667959 | AGCACTGCCCCAGCC[C/G]GCCTGAGGCCAAAGG | 6468 |
rs141291122 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646861 | ATCATAAATAGCCTA[C/G]AGTGATCCCACAGCT | 6468 |
rs141294574 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622559 | AGTGAAATCCTGTCT[C/T]TACTAAAAGATACAA | 6468 |
rs141354974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647506 | ACTCACACCACACCA[A/C]CACTTGCTTTGGAAT | 6468 |
rs141526805 | in-del | -/A | 0.319376 | 0.240181 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666925 | AACAAAAAAAGAATG[-/A]AAAAAAAAACCACCC | 6468 |
rs141558311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670186 | AAAATAATCCTAAAA[C/T]AAAAGAAAAACCTAA | 6468 |
rs141584853 | in-del | -/TTAT | 0.122758 | 0.215196 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680060 | GTTGCACAAAAGTCA[-/TTAT]TTCATTCCTTTTTAT | 6468 |
rs141657077 | snp | A/G/T | 0.000115706 | 0.00760532 | missense, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611628 | GGGCAGGACACTTAC[A/G/T]TGCAGGCAGGCCCTT | 6468 |
rs141665192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662307 | AGTACACAGTGATTG[C/T]TTTCCTTCCAGACGC | 6468 |
rs141761521 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620182 | CTCACCGCCCAACCC[C/G]AAGTCCTGCCGGCAA | 6468 |
rs141845017 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626346 | TCCCCAAACATTTTT[C/T]TATTTAGGGTAATCC | 6468 |
rs141881853 | snp | A/T | 0.0489665 | 0.150044 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631874 | CCTTGTGATCCACCC[A/T]CCTTGGCCTCCCAAA | 6468 |
rs141919823 | in-del | -/ATAAA | 0.0310518 | 0.120672 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670946 | ACTTCCCTTTACCCC[-/ATAAA]ATAAATCTCTTTCCT | 6468 |
rs141998785 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613706 | GAGCTGCCATCTTCC[C/T]GAAGGCCGAAGGAAT | 6468 |
rs142079493 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692624 | GCTGGGTGTGGTGGT[A/G]CATGCCTGTAATCCC | 6468 |
rs142098066 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625057 | TGGGCCTGCTGCACA[A/G]ACTAGGTTGAGTGGT | 6468 |
rs142121812 | snp | A/G | 4.95593e-05 | 0.00497767 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611320 | AATCCAGGACGTGGA[A/G]GTTGTAAGACAGGGC | 6468 |
rs142182015 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636915 | TTAAAAAGTATCACT[A/G]TCTTTTAGAGTACAG | 6468 |
rs142205466 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615790 | ATAGCCCGCCAGGGA[C/T]AGGCCCTGAGTGCTA | 6468 |
rs142256886 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656400 | GAGAGGAAAAAGGCC[C/T]GGTGGCCTCACATTC | 6468 |
rs142294631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660631 | ATCTGTTGGCAGAAC[A/G]GTGATCAAAGGTGGA | 6468 |
rs142390940 | in-del | -/ATAGA | 0.0535932 | 0.154675 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678930 | CACTTATTTATTCAT[-/ATAGA]ATAATTATTTTTGGT | 6468 |
rs142393975 | snp | C/T | 0.000632479 | 0.0177719 | intron-variant | FBXW4 | GRCh38.p7 | 10:101611596 | AATCATGAGTCCTGG[C/T]ATGCTGGAGAAGAGG | 6468 |
rs142513051 | in-del | -/T | 0.0130921 | 0.0798413 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610539 | AAAAAGAAACCTTTG[-/T]TTCTTTGGGACACAG | 6468 |
rs142529773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630994 | CAGTGGCATCTGTTT[C/T]GAAAGAAGGAAGGGA | 6468 |
rs142622374 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684348 | AGCCAGGATAGTCTC[G/T]ATCTCCTGACCTTGT | 6468 |
rs142654224 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695929 | TGCACACCAGATTTT[A/G]AAGCCATACAAAAAA | 6468 |
rs142665523 | snp | A/G | 0.021333 | 0.101051 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635165 | AGGAGCACAAACCCT[A/G]TTGTGAACTGCACAT | 6468 |
rs142732621 | in-del | -/A | 0.204189 | 0.245767 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682420 | ACTGAAATCTAAATG[-/A]AAAAAAAAATAGACT | 6468 |
rs142753284 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656715 | AGGAAGAGGCAGCAG[C/G]GCAAGCTAAGCAGGC | 6468 |
rs142756910 | snp | A/T | 0.128632 | 0.218563 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654017 | TCCCAGCTACTTGGG[A/T]GGCTGAGGCAGGAGA | 6468 |
rs142796080 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650847 | CGTGAACACACAAAA[C/T]TGACAGGGCAGAGGG | 6468 |
rs142804331 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642248 | ATACACATTTAAAAA[C/T]TGAAGCAAAACATGA | 6468 |
rs142870264 | snp | C/T | 4.94319e-05 | 0.00497127 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624792 | GTGCCCGCAACAAGC[C/T]GTCCCTGTCACAAAA | 6468 |
rs142927609 | snp | A/G | 4.94434e-05 | 0.00497184 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611673 | CAGCCGTACAACACC[A/G]TAGTAGGAGGAACCT | 6468 |
rs142972949 | in-del | -/AAAAC | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641636 | ATTTTTTCTCAAAAA[-/AAAAC]AAAACAAAACAATAC | 6468 |
rs143025894 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613325 | ACATCAAGTGCACCC[A/G]CTAATCCCTGCAGCC | 6468 |
rs143070541 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663280 | TGTGCCTATCATCTC[C/T]CCACCACTGAATAAG | 6468 |
rs143070839 | snp | A/G | 0.000512392 | 0.0159979 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676407 | TTCTGAGACACCTTC[A/G]CTCGTTCCTTCACTG | 6468 |
rs143071613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678793 | TTTTACTAAAAGCCA[G/T]CAAGCAAGTCCAGCT | 6468 |
rs143111364 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614718 | TTTCTTTTGCCCCTG[A/C/G]GCCCAGGACCCTCAA | 6468 |
rs143263487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620209 | GCAATGCTGCTCCAC[C/T]TCTCGGATTGGCCTG | 6468 |
rs143359606 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639289 | CACATTAGAATATGG[C/T]GGGTTTTGCTAAGGA | 6468 |
rs143368749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619180 | TACTTCAGTGGTTGG[C/T]CAATCAAGATGAAGA | 6468 |
rs143417015 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681010 | TTTTGGCAACAACTA[C/T]AGCAAGTAATGGTAT | 6468 |
rs143455716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690650 | CAACAAAGCTATGAT[C/T]AGTTAGGAACAGCCA | 6468 |
rs143535850 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643143 | TCCGCCCAGGCCACT[A/G]ATTCCTTTACTGCTG | 6468 |
rs143549157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662127 | TTCCAATCTTTCAAA[A/C]CTCTCTGTCAGAGAA | 6468 |
rs143654608 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654830 | GGTTTCTTTTGGTTT[C/T]GTTACTTTTTTGAGA | 6468 |
rs143678026 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648752 | CATTCCACCATTTTA[C/T]CCTTTTAATACAAAA | 6468 |
rs143749431 | snp | A/C | 1.65255e-05 | 0.00287445 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611348 | GGCAGCATAGAGATG[A/C]TTGGTGGTGAGACGC | 6468 |
rs143859921 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657326 | GACAAGAAATAAAAC[A/G]CCTACTTCCAAAAGC | 6468 |
rs144016365 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682578 | TCTGGATCATAGCAG[G/T]AAGAAAACGAAAGTA | 6468 |
rs144041573 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677256 | TCATAATAGCCAAAA[C/G]TGGTAAACAGCCCAG | 6468 |
rs144090968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691648 | TGAAAATAAACATCA[A/G]TTCTTTCATTCATTC | 6468 |
rs144112153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624130 | CACACAGAGTGCAAT[C/T]TGAATAAAGGTCCAT | 6468 |
rs144131587 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629574 | GACGCATGAGCCACC[A/G]CACCCAGCCCCACTT | 6468 |
rs144193696 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680567 | GTCACAGTGTTCACA[A/G]TATAAAACATTGGAG | 6468 |
rs144230287 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101644040 | CCCCCATCCCACATT[C/T]GTACCTGGGCTCTCC | 6468 |
rs144297128 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101638298 | TGGTAGGATGGGGTG[C/T]TCTGACATGAAAGGA | 6468 |
rs144381704 | snp | C/G/T | 0.104504 | 0.2033 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654095 | CACTGCACTCCAGAC[C/G/T]GGCGACAGAGCGAGA | 6468 |
rs144438503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653044 | CTGGGCTGTCTCTGG[A/C]CATTGCCACCTGACT | 6468 |
rs144453372 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651094 | CTCTGCACATTCCTT[C/T]GAGAAACAGGAGCAC | 6468 |
rs144478868 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657371 | GGCACGGTGGCTCAT[G/T]CCTGTAATCCCAACA | 6468 |
rs144561174 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642831 | TGCCATGCCCACCAT[C/T]AGCGCCACCAGGCCC | 6468 |
rs144609481 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665951 | ACCACCACCTCCACT[C/G]CAGTCTCCCAAAACC | 6468 |
rs144637047 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668066 | GAGGTGACTGTTGGA[A/G]GTGGAGAAATGGGGA | 6468 |
rs144646260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671937 | ATAAAAAGAAGGGAA[C/T]ATATTTAGCCCTTCT | 6468 |
rs144754776 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687382 | AGCCAGTGAGCATAA[C/G]ACTTCTCTTTCTCTA | 6468 |
rs144777520 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675047 | TTCTTCCCCAGACTC[A/G]TACAAGTGTCATGGG | 6468 |
rs144779083 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664822 | GTGAAACCCTGTCTC[A/G]ATATGCATAACACAT | 6468 |
rs144978122 | snp | A/C | 0.000439271 | 0.0148136 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612408 | CAGTGTGAAAGGGGA[A/C]TCATACATGACATCC | 6468 |
rs145006189 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101647016 | CAAGCATGGCTTCAG[C/T]CAGCGATACCACAAA | 6468 |
rs145087787 | in-del | -/AC | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101632212 | CCACACATATTCTCT[-/AC]ACACACACACACACA | 6468 |
rs145158495 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681401 | CTCAAAAAAAAAAAA[-/T]TAATAATAATAATAA | 6468 |
rs145177493 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672951 | GCCACTCACAATGAT[A/G]CCCCCTTTGCAATCC | 6468 |
rs145183921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615510 | ACCTGGGGGAGACCT[A/G]TTTCCTTGGCTCTGA | 6468 |
rs145220114 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669899 | AGCTGGGTCTACAGG[C/T]GCCTGCCACCATGCC | 6468 |
rs145250200 | snp | A/G | 0.000465573 | 0.0152502 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612399 | ACAGGACAGCAGTGT[A/G]AAAGGGGACTCATAC | 6468 |
rs145262524 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675887 | TACCCTGCCTTTTAA[C/T]AAAGTAGGGGAGAGG | 6468 |
rs145442760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616725 | GCTTGGGAGTGTGCT[A/G]GCAGGGTCTGGCCTC | 6468 |
rs145665006 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641675 | CTTAAGTGTGTCCCC[C/G/T]CAAACCCTCTCACTC | 6468 |
rs145666220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624015 | ACAAACAGTTCTGTA[C/T]CTCAATTGTGGTGAT | 6468 |
rs145784702 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 10:101645987 | TGATGGTACCTATCT[A/G]GGGGGATTAAATAAG | 6468 |
rs145813139 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645356 | TGAAACGGTTTGCTC[A/G]GAACAACTGGCTTGG | 6468 |
rs145967625 | in-del | -/AA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637721 | AAAAAAAAAAAAAAA[-/AA]GGTCACTATGAGGTT | 6468 |
rs146005348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629981 | CCCAGCTGGCCCAGG[C/T]CCCAGCAGCCTCTGA | 6468 |
rs146017244 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635743 | CAGGAGGGTGAGGTG[A/G]GAGGATCTGATCCCT | 6468 |
rs146062180 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660796 | GCAGTGGGAGGAAGA[A/G]AAAGATGACTGATCC | 6468 |
rs146124624 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658237 | AAGGGAGAGGGAGGC[C/T]TATTTAAAAATAAAA | 6468 |
rs146166302 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101663354 | CAAGGAGTGAGGTGA[A/G]AGGGTGAGAAGGGAA | 6468 |
rs146206634 | in-del | -/AGG | 0.0524604 | 0.153226 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655688 | AAGGCGGAAAATAGC[-/AGG]AGAAGGAAACACCCT | 6468 |
rs146295152 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629121 | GAAATTAGTTGGGCA[C/T]GGACAGCCTGAAAGG | 6468 |
rs146307220 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633561 | TGTAACAAACCCGCA[C/T]GTTCTGTACATGTAC | 6468 |
rs146469941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617083 | TGGCAGAGTAGCCAC[C/T]GCAGCAACAGCTCAC | 6468 |
rs146481624 | snp | C/T | 0.0010596 | 0.022993 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624857 | TGGCTTGTCAGAACC[C/T]GTGGTGGAAATGGCT | 6468 |
rs146590579 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646804 | TGGGGTATTTAGTTG[C/G]TTTGAAAAAATAATC | 6468 |
rs146597422 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653046 | GGGCTGTCTCTGGCC[A/G]TTGCCACCTGACTGT | 6468 |
rs146703913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675227 | CACTCATTATGCACA[C/T]TCCTCTTCAATATCC | 6468 |
rs146716253 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681094 | ATTATGTCTCCATAA[A/G]TAACAGGTCTAGGCT | 6468 |
rs146792313 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684835 | TATCATGTTAAATTG[C/G]TTATCCTTTTGGCCA | 6468 |
rs146885567 | snp | A/T | 0.000280114 | 0.0118313 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101672987 | GTTCACCTCCTGTTC[A/T]TGAGCCGAGTACTTG | 6468 |
rs146893502 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695995 | GATTACGTGTTGAAG[C/T]GTTAATATTTTGGAT | 6468 |
rs147071681 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101622156 | TAGAATGGATTTTTC[-/A]AAAAAAAAAAAAAAA | 6468 |
rs147177413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643524 | CGCAGGCATATGCAC[A/G]CTTTGCATTACATCT | 6468 |
rs147187407 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101649785 | GCCACCTCATCTCAG[C/T]GGCCAGCCTGCATCT | 6468 |
rs147282508 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671644 | AGATGGCTAGAATAA[C/G]ACAGGAGTACCTAGG | 6468 |
rs147293065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677430 | TTACACAAAAGAAAT[C/T]GTAGTGTATGATTTC | 6468 |
rs147424741 | snp | A/G/T | 0.000264764 | 0.0115029 | missense, synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611739 | GTACAGGGTGCTGTC[A/G/T]TGGGGCTCCTCCCAC | 6468 |
rs147458519 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679087 | TATGTATTCACTGTA[C/G]ATAAGTATATATGCA | 6468 |
rs147494591 | snp | C/T | 0.015463 | 0.0865586 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615101 | TTGCAATTTGTATAA[C/T]GTGGTGACCCCCCAA | 6468 |
rs147554097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631546 | AATGATAAGCAATTC[C/T]TTCTTCTTTTAAATT | 6468 |
rs147563194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638103 | GCATGATCTTTCTAA[A/G]TGTCTTTCCTGGAAA | 6468 |
rs147658251 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660623 | GCTAAATTATCTGTT[A/G]GCAGAACGGTGATCA | 6468 |
rs147667651 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665468 | GCCAAGAAGAGGACA[C/G]GAAGACCCTGAAGAT | 6468 |
rs147757900 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638517 | AAAGAGTAGGATAAC[A/G]GGAGGGGACACAGGT | 6468 |
rs147862540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666187 | CTCCACTCCCTGCTG[A/G]TCTTTCCTTCCCTCT | 6468 |
rs147872277 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672184 | CCTCCTGCACCACCA[A/C]CTGAATTGTCAGCAA | 6468 |
rs148012023 | snp | C/T | 8.27369e-05 | 0.0064313 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611361 | TGCTTGGTGGTGAGA[C/T]GCAGGCAGTACACAG | 6468 |
rs148076154 | in-del | -/T | 0.332337 | 0.236052 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636589 | ATTATGATTACTATC[-/T]TTTTTTTTTTTTTTT | 6468 |
rs148112767 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687435 | CACAAAATCAACAGC[A/G]TACCCTAATCCAAAA | 6468 |
rs148163606 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677182 | TGTGTACTCTATGAC[C/T]TAGGAATAACCTTAG | 6468 |
rs148174377 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613688 | CCTCCCTTCTCCCCA[A/G]CAGAGCTGCCATCTT | 6468 |
rs148292366 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647159 | CATGTTTTCTGGGTC[C/T]CAGGCCTGGGCAGGG | 6468 |
rs148390480 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651109 | CGAGAAACAGGAGCA[C/T]ACCAGTCTCTGAGCC | 6468 |
rs148443249 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642926 | GGTACGCACATACAT[A/G]CATACCTGTAAACTA | 6468 |
rs148485518 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672377 | TTCTTTTATGCCTTG[A/G]TGGATATCTGTGGAC | 6468 |
rs148535514 | snp | A/G | 0.000115334 | 0.00759299 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101624783 | GGGTGAGAAGTGCCC[A/G]CAACAAGCCGTCCCT | 6468 |
rs148685697 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680773 | CTGTTAAGACAAAAG[C/T]CATTAAATGACAGCT | 6468 |
rs148687722 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636236 | GTGGCGTGCACCACC[C/T]AACTACTCAGGAGGC | 6468 |
rs148694939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615524 | TGTTTCCTTGGCTCT[A/G]ACCGTGTGCAGGCTG | 6468 |
rs148845366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630572 | ATTACAGCAGTAAGT[C/T]CCAAAGCATGAATAC | 6468 |
rs148887425 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662073 | CTGCAGCACCACTGG[C/T]AACCAAAAGAATCTG | 6468 |
rs149053406 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692045 | ACAGATATGTAAGAA[C/G]TTTATCATGAAAACC | 6468 |
rs149060278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668046 | GGAGGAGAGGTGCTC[C/T]GGGAGAGGTGACTGT | 6468 |
rs149070050 | snp | C/T | 8.26221e-05 | 0.00642684 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101676377 | ATCCCCTCTCGGCAG[C/T]GCCCCAGTCTCCAGT | 6468 |
rs149212193 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639277 | CTCTGTGCATGTCAC[A/C]TTAGAATATGGCGGG | 6468 |
rs149315655 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642748 | CACCTCTTTGGAACA[C/T]TGGAATAAAGGCCAA | 6468 |
rs149372893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632753 | AACAACTGTTCCATG[C/T]GCTCCTAAAATAAAG | 6468 |
rs149412228 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664579 | GGGCAGGAACACTAC[A/C/T]GGGGGAAGAGAGATT | 6468 |
rs149431155 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676618 | CAAGGAGAAAAGCCT[A/G]TCCTTTAAACTATCA | 6468 |
rs149469501 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657093 | CCCTCCAATCCTCCC[A/G]CCCTTGTCAGCACCT | 6468 |
rs149589501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627889 | GCTTTGAAAAGGGGC[C/T]GGTGGGGTGGGATCT | 6468 |
rs149590377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671266 | GAAGTCACAGGGGAG[A/C]TGCAAACCAGCTGAC | 6468 |
rs149645692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618497 | TGAGAAGCCTATTCT[A/G]CCCCTGCCTTTGTTG | 6468 |
rs149694766 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630179 | AGCTCTCTGACCTCT[G/T]ACAGGCACTGACACG | 6468 |
rs149786806 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653865 | CAGTGGCTCACGACT[A/G]TAATCCCAGCACTTT | 6468 |
rs149791990 | in-del | -/CA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612824 | ATTCACATGCACATG[-/CA]CACACACACACACAC | 6468 |
rs149844126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645283 | TTGGGGGGAAGCCCA[A/G]TCCAACAACCTGCCT | 6468 |
rs149981215 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680564 | ACAGTCACAGTGTTC[A/T]CAATATAAAACATTG | 6468 |
rs150033036 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624091 | ACATAGACACAGACA[C/G]ACACACACACACACA | 6468 |
rs150086197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683798 | TGCTGACCAACTGCA[C/T]GGATGGCATGATTTC | 6468 |
rs150096317 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618352 | GATCAAGGAGAGCTT[C/T]GTGGTGGAGGTGCTG | 6468 |
rs150244056 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632716 | AGTTTCTAAACTGGA[C/T]TTCCATCTACATGGC | 6468 |
rs150296968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625866 | GCAATGTGGGGGCAA[C/T]AGCCCATCTGCTGTG | 6468 |
rs150365665 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648286 | TGGGCCTTTGATGAA[A/G]TCACAACAAGCATTG | 6468 |
rs150456583 | snp | C/T | 0.000131778 | 0.00811614 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673534 | GCACAAAGTGGCAAA[C/T]GTCCTCATCATGCCC | 6468 |
rs150515781 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101662720 | TGTCTGCAGAGGGAC[A/G]AGGAGCTGTGGGCGC | 6468 |
rs150521753 | snp | G/T | 0.000148523 | 0.00861624 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611638 | CTTACGTGCAGGCAG[G/T]CCCTTTGACGCCGGT | 6468 |
rs150611589 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690058 | TTAATTCGGGAGGAA[G/T]AGGATCAAGTAAGCT | 6468 |
rs150670406 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613736 | TCAAAGGAGGAGACT[C/G]GGGGTTCCTTTCTGC | 6468 |
rs150733613 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656924 | CACCTGTCCCCCCTA[C/T]ACTTTTCTGTGCCCA | 6468 |
rs150768038 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636989 | CAAAATAATATGGGA[C/T]GGGAAAGTGTGTAGG | 6468 |
rs150883374 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670859 | AAACCTGAAACTGGG[C/G]TTGTGGGGAGGGGAA | 6468 |
rs150915058 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651716 | GACCCCCACCCACTG[C/T]TTGCTTTTGTACTCT | 6468 |
rs150933188 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682586 | ATAGCAGGAAGAAAA[C/T]GAAAGTAAAAGAATG | 6468 |
rs150986453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674716 | TACAGAGAAAGTCAG[C/T]TCTCACAGGCAACTG | 6468 |
rs151048089 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, intron-variant | FBXW4 | GRCh38.p7 | 10:101667940 | TCAGTCTGGATGGTG[C/T]GTAAGCACTGCCCCA | 6468 |
rs151092322 | in-del | -/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101650562 | AACTAACCGCCCCCC[-/C]TCAAGGGGTGGTGGG | 6468 |
rs151143544 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625403 | ACTACATAGGTGGGG[C/T]GGAGTCCCCAGAAGC | 6468 |
rs151196822 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615982 | CAGCTCAGCATGTCC[A/G]TGGCTCCCACACCAT | 6468 |
rs151286703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658643 | CTCCAAGTGGCCTGA[A/G]AGCCACCTAATTGCA | 6468 |
rs151291220 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639465 | CCATTCACATAGACA[C/T]TTTGGGACTGGACAT | 6468 |
rs151303821 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101644249 | GCAAGCCAAACAAAA[A/G]AGGACTCTGAATTGG | 6468 |
rs180797980 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101613713 | CATCTTCCCGAAGGC[C/T]GAAGGAATCAAAGGA | 6468 |
rs180921428 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666330 | AATGGGGTCTCCATT[C/T]TCCGGGGTCAGCAAT | 6468 |
rs180931033 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635760 | AGGATCTGATCCCTT[A/G]AGCCCAGGAGGTCAA | 6468 |
rs181096007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619425 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 6468 |
rs181119596 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101680895 | ATATTAGAGCTAAAA[G/T]CTGGAAATAGCCCGA | 6468 |
rs181131728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657365 | TGGCCAGGCACGGTG[A/G]CTCATGCCTGTAATC | 6468 |
rs181133299 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631829 | AGATGGGGTTTCGCC[A/G]TGTTAGCCAGGATGG | 6468 |
rs181293023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648982 | ATGCTCCAAACTCTG[C/T]TTTAAATCCCTGGGT | 6468 |
rs181352274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626832 | CTGACTGGCCACAGG[C/T]CTAAATTAGCATCAA | 6468 |
rs181426197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612192 | TGCCCAAATGTAGGA[A/G]GTCTAGTGACCTTGC | 6468 |
rs181463660 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665237 | TACACTCTGGTCATC[G/T]AGTGTAAAGACAGAA | 6468 |
rs181476366 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631666 | AGAGTCTCGCTCTGT[C/T]GCCTAGGCTGGAGTG | 6468 |
rs181584778 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679698 | TATTTTCTCCTTTAT[A/G]CTTTTACATATTTTC | 6468 |
rs181590797 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101655497 | TCAAAGGCATTAACA[C/T]ATGTGTGTCTTCCTC | 6468 |
rs181593643 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685067 | AGCCAATCTCTTCCA[C/T]GTTCATTCATATACC | 6468 |
rs181601304 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635318 | TCTACATTATGGTGA[C/G]TTGTATAATTATTTC | 6468 |
rs181726096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625814 | TGCATGTCTTTCATG[A/G]GGGGGAAGGAAGACT | 6468 |
rs181766139 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641938 | TTGGGAGGCTGAGGC[A/G]GGTGGGTCACCTGAG | 6468 |
rs181797338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666525 | ACGAAGTGGGTAGGA[C/T]CAAGTCTCTTATAAA | 6468 |
rs181800505 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691913 | TCAAAATTTACAAGA[C/G]TAGAGTAATCTTCTA | 6468 |
rs181901612 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686438 | CAACTTTTGGAAAGG[C/G]TGATCTAGTACTTTC | 6468 |
rs181940879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636656 | GTAATGGTGCAATCT[C/T]GGCTCTCTGCAACCT | 6468 |
rs181956236 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FBXW4 | GRCh38.p7 | 10:101674146 | ACCAGCCTGACCAAC[A/G]TGATAAAACCCCGTC | 6468 |
rs182000143 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658577 | GTTTGAAATGAAAAA[G/T]AAAATGAGGAAGGTA | 6468 |
rs182018741 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631870 | CTGACCTTGTGATCC[A/G]CCCACCTTGGCCTCC | 6468 |
rs182018765 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101691030 | ATTTTACCAGGCAAG[A/G]TTATTCCCATTCTTT | 6468 |
rs182048262 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621067 | GGGCCCAGGCAGGTG[A/G]TGATGCCAAACACAA | 6468 |
rs182069001 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670044 | ACAGGTGTGAGCCAC[C/T]GCGCCCGGCCGGGAG | 6468 |
rs182205647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648421 | GATTTGATTGACTAG[A/G]CAGAACTTAGGTAAG | 6468 |
rs182208577 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688400 | GGGCTAAAGAGGGGC[A/C/G]GCAGGCACAGGGGCC | 6468 |
rs182221857 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696637 | CAAAGACTTTGTGTA[A/G]AAAACGATTTCCAAA | 6468 |
rs182222827 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667304 | AAAAAAGAGAAGTAA[C/T]AATCAGACCAAAGGG | 6468 |
rs182235569 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614900 | CCGTGGGCCCTTCTC[A/G]GCCCCCACCCCAAGA | 6468 |
rs182266366 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639682 | AGTCACTCTCTCTGA[G/T]TTAAGCCATGAGCTG | 6468 |
rs182270098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616948 | TAAAGGCAGAGCTCC[C/T]GGAAATCCCGTCTGG | 6468 |
rs182327566 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101620785 | GCCTGGCTAATCACT[C/G]TCTCATACCTATTCT | 6468 |
rs182391069 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622139 | TTTGAAAAGACTGAC[C/T]ATAGAATGGATTTTT | 6468 |
rs182484631 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692255 | ACAATGAAGAGTTCA[A/G]ATATAGATCCAATAT | 6468 |
rs182491271 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682257 | GAACAATTAGGACTT[A/G]GCTATACACATGTTA | 6468 |
rs182500638 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643202 | ACATGGGAGCAAGAT[G/T]GTAATGATTAGCGTA | 6468 |
rs182504691 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671803 | GGGTAATAGGAAGCA[A/C]GTGACAGGAAATTCA | 6468 |
rs182588925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641458 | CTTCTTTTATCTCTT[C/G]TCCACCCTGACCTGG | 6468 |
rs182668753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651076 | GACCATTAATGCATG[C/T]GCCTCTGCACATTCC | 6468 |
rs182791436 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653861 | GGCGCAGTGGCTCAC[A/G]ACTGTAATCCCAGCA | 6468 |
rs182800907 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629343 | AGGCTGGAGTGCAGT[A/G]GTGCAATCTCAGCTC | 6468 |
rs182904413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | FBXW4 | GRCh38.p7 | 10:101628004 | TCGATTTGAATCCGC[A/G]AGATGTCTTCAACCA | 6468 |
rs182916740 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677593 | AAGTCTTGAGGGGGT[C/T]TGGGTTATACAAGTT | 6468 |
rs182927771 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101675425 | TTATTTGCCAAACTG[A/C]TTGAAACTAGCCCCA | 6468 |
rs182953023 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101633743 | ATATACCAGCAATAA[A/C]CAAGTGTTATTATAT | 6468 |
rs182999397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101683582 | ACCTTTCATTTCCCC[C/T]CTCCTTGCTCACACC | 6468 |
rs183052259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682451 | TCCCTGTCTGCTCCT[C/T]GTATCTGCAAATCCC | 6468 |
rs183053669 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623005 | ATGAACAGACGTTTC[A/G]CCAAAGAGAATATTC | 6468 |
rs183110667 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660164 | TAAGAGGAGAAAGAG[C/G]TCCTACACAGCACCT | 6468 |
rs183113766 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632261 | CCAAGTGCATCAGGG[C/T]AGGATGGTGCAAGTA | 6468 |
rs183119589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615823 | CTGGACTGGGCACAG[A/G]GGGCAGTCCCTGGCA | 6468 |
rs183225106 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688552 | AGTCTCATACTCATT[C/T]TTAGAGAAAGCTCAA | 6468 |
rs183234328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661596 | CTTCCATCTTTCTCC[A/G]GGTGTCATGACGCCC | 6468 |
rs183342025 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651893 | GAGATGAAAGGGGGC[A/C]GCGGCCCTCTCCCTG | 6468 |
rs183344531 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628436 | TCTCCCCTTTGAGAT[C/T]AGAATCCTTTAGAGG | 6468 |
rs183399170 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692408 | AGACAACAATAGTAA[A/G]TTGAATTCACCTCTT | 6468 |
rs183415364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687452 | ACCCTAATCCAAAAT[A/G]CTTGCTTCCGGCCCA | 6468 |
rs183453371 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101646549 | GTTGCTGGTCAAGGC[A/G]CCTTTGCTTGCTTGG | 6468 |
rs183479036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693453 | CCCACAAACATTTAC[C/T]ATGTACCTATTCTGT | 6468 |
rs183499375 | snp | A/C/G | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684373 | CCTTGTGATCCACCC[A/C/G]CCTTAGCCTCCCAAA | 6468 |
rs183508988 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663982 | GAAAAGGTCCTTGCC[A/T]GCCACTTTCCTTTGG | 6468 |
rs183684010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672488 | GAAGCAGTGAAAACA[C/T]ATTTTAATTATCAGC | 6468 |
rs183827024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669406 | GCAGATTCTTTCTTA[A/G]GGGGTGAGGAAACAC | 6468 |
rs183827222 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101676218 | CCTTTGTGTTATTCA[A/G]AGGCTCACCAGTGCC | 6468 |
rs183834788 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640870 | AAGTCTCACTCTGTC[A/G]CTCAGGCTGGAGTAC | 6468 |
rs183839116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101619934 | TGAGAGACACACATA[G/T]ACGTGGGTGATGGCT | 6468 |
rs183941896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689810 | CTCACCACTCTGGAC[A/G]TTAATCATCACTGAA | 6468 |
rs183997212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622503 | GAGGCCGAGGCAGGC[C/T]GATCACGAGGTCAGG | 6468 |
rs184033371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672302 | CACAGGTGGAAGCCT[A/G]TTTGATCCAGATGTG | 6468 |
rs184044682 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667719 | AATCCCACGCATATA[C/T]GAAGTGGCCTAAATA | 6468 |
rs184089480 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695465 | TGGCCTTGCCCCTCT[A/G]GAAGCCCTCCTCTTC | 6468 |
rs184150913 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646690 | TGTTCAGCACAGTAA[C/T]CCAAAGGAGGCTGGA | 6468 |
rs184155184 | snp | G/T | 1.69206e-05 | 0.00290861 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673066 | GGAGAGAAATAAGGA[G/T]CCGACCCCCAAGAAC | 6468 |
rs184170966 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625098 | CATAAAAACAGATCT[C/G]TAGACGTGACAAGTT | 6468 |
rs184175748 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101624058 | CTACACGTGATACAA[C/T]TGCAAAGGACTAGAC | 6468 |
rs184200725 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673373 | CTTTAAATGGAAAAC[C/G]CTTCTGGTCTCCCTC | 6468 |
rs184232718 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680344 | TAGAAATGTATCAAT[A/T]ATAAAGTATTTGAGT | 6468 |
rs184249144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656171 | ACTGCCTTTTGGCCT[A/G]TTTTTGTGTCTTCTT | 6468 |
rs184287742 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618507 | ATTCTGCCCCTGCCT[G/T]TGTTGAGAAAAGGGG | 6468 |
rs184306328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647523 | ACTTGCTTTGGAATC[A/G]ATTTTTTTTCCCCCA | 6468 |
rs184353164 | snp | A/G | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695932 | ACACCAGATTTTGAA[A/G]CCATACAAAAAAAAG | 6468 |
rs184359830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654301 | ATGGAATTGTGGTGA[C/T]AGTTGCACAACTTTA | 6468 |
rs184361120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684599 | ACACTATCTCTTGAT[G/T]TCTCTTATCTTCTTT | 6468 |
rs184377885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664582 | CAGGAACACTACAGG[A/G]GGAAGAGAGATTCCT | 6468 |
rs184484399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630233 | GCTTTTTATCTGAGC[C/T]TTATTACTCTCTATT | 6468 |
rs184514753 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678373 | GACAAGAGTGATAAC[C/T]GCCATGTCTGCCTGG | 6468 |
rs184625996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654700 | CACAATCTGCTATGA[C/T]ATCTTTTGGTTCCAT | 6468 |
rs184628169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101679067 | TCTCCCTCTCTAGAG[A/G]CAACTATGTATTCAC | 6468 |
rs184654497 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685474 | CAATTTTACAGGGAT[C/T]TCTATCAGACACTAA | 6468 |
rs184673383 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635634 | GAGCCCAGGAGTTCA[A/G]GACAAGCCTGGGCAA | 6468 |
rs184695522 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631353 | TGGAATATTATACAG[C/T]CCTTTTAAATGATGT | 6468 |
rs184800246 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665607 | TAGTAGTGGCAGTCA[A/T]GTAGTAGCAGTAATA | 6468 |
rs184811499 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634769 | ACATTTTTAAACTGT[A/T]TGAAAACCCATAAAG | 6468 |
rs184823378 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610497 | CAAAGGGTAAGGGAT[A/G]GGTCATCAATGGGAA | 6468 |
rs184861041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612794 | GGGCTTGCTGAAGGG[A/G]TCGGCCCCCCTCACA | 6468 |
rs185025596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668152 | CTTCTGGCTCACCTA[C/T]CCCCGCAGATAGGCC | 6468 |
rs185027627 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631667 | GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAGTGC | 6468 |
rs185133251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686053 | ATGTCAAAAATGTCT[A/G]AACAGTTTCAGAAGC | 6468 |
rs185140274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689148 | GCAAAAAAAAAAAAT[A/G]AAAGTATGGAGTACC | 6468 |
rs185146449 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640562 | AGTGGCATGATCTTG[G/T]CTCACTGCAACCTCT | 6468 |
rs185181909 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611087 | GTCCTGCCTCTCCAA[C/T]AGGTTCCTGGGAGGG | 6468 |
rs185191197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666390 | AAATTGAAGAATTAA[C/T]GACGTGGCTAATCGG | 6468 |
rs185205519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636076 | CAAATTAGGCCAGGC[A/G]TGGTGGTTCACACCT | 6468 |
rs185211426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614640 | AGTTTCTTTCTGCTG[C/T]GCTGTTCTCTGGTTC | 6468 |
rs185229715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622292 | GTGGCATTTAAGACA[A/C]AGACCACATGTGGGG | 6468 |
rs185254951 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692256 | CAATGAAGAGTTCAG[A/G]TATAGATCCAATATA | 6468 |
rs185264109 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643735 | AGTCTCTGTCCCTCC[C/T]TCTTCCCTCCCACGG | 6468 |
rs185264298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672225 | GCAACCCTAAAGGAC[C/G]AGGCCTGTGCAGGCC | 6468 |
rs185328100 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635003 | CAGACCTGTACCAGT[C/T]CATGGCCTGTTAGCA | 6468 |
rs185370446 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627073 | TTTTTTTTTAAATAG[A/C]GACAGGGGTCTCACT | 6468 |
rs185397857 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675244 | CCTCTTCAATATCCC[C/T]TTGCGTGAGTGTGTG | 6468 |
rs185407024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650549 | GCCCTATGGGGTAGA[A/G]CTAACCGCCCCCCTC | 6468 |
rs185552251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639872 | TTCTGCCTTTGGCTT[A/G]GTTTTTCACCTTTTC | 6468 |
rs185638932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617336 | GCCCCTCAACATCCT[C/T]AGGACTTGCCCCAAG | 6468 |
rs185746502 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101642115 | AGGTTGCAGTGAGCC[A/G]AGACTGTGCCATTGC | 6468 |
rs185750591 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621216 | TAGTCACTAAGACAC[A/G]GATATTTTAAGAATT | 6468 |
rs185756024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675464 | ATGTGGGAAGCAGAG[A/G]GTAAAGTCCTTCATC | 6468 |
rs185775057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628126 | TGTATCATTCCCTCC[A/G]TGGCTCCTCCCAAGG | 6468 |
rs185899209 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648625 | AGAAGTTAATGTGCA[A/T]CCAACCAGGCCCAAT | 6468 |
rs185899498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101625930 | AAGCATGTCAGTGAG[A/G]AGATGGATTTCCACA | 6468 |
rs185907584 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101651284 | TAATTACTCGCCTAC[A/G]CTCTGGAGCGCCCAG | 6468 |
rs186123103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101657742 | GCAGATGTCCAATCC[A/G]TAGTCAGAGACCTTT | 6468 |
rs186244278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681025 | TAGCAAGTAATGGTA[C/T]TTTTAAAACTAAGTT | 6468 |
rs186255077 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631851 | CCAGGATGGTCTTGA[C/T]CTCCTGACCTTGTGA | 6468 |
rs186284639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686690 | AAACTGTGTTCTATA[C/T]TAATCATCAAAACAG | 6468 |
rs186380826 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101659122 | GGGCCTCTGTCGGCC[A/C]GTGTCCCAGATTAAT | 6468 |
rs186387383 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682272 | GGCTATACACATGTT[A/T]AGGCTAAAATCTTTT | 6468 |
rs186390063 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632049 | CAACCATGGCCCTGG[C/T]ACACCTTGCCCTGAA | 6468 |
rs186436107 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101687815 | ATCATCATACACTAA[A/G]TGCTCTTCAATTCTG | 6468 |
rs186462621 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639740 | ATGGAATAAGCTGGT[C/G]AGCTTGGAGAAAGGA | 6468 |
rs186466165 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617275 | TATATGCTTCAGGGT[A/G]GTGGCACTCCCCACC | 6468 |
rs186480544 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688486 | AGAAATGACTCAAAA[C/T]TGAGACAAGGCAGCC | 6468 |
rs186512810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667537 | TGCTGTCACCTCCGA[A/G]AGGTGGTGAGAGGCC | 6468 |
rs186546887 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101670972 | CTCTTTCCTAAAATA[C/T]AGTACATATTTGGGA | 6468 |
rs186773132 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691963 | AGAAAACATACTGAA[G/T]AGAGTGTATTTGCAA | 6468 |
rs186929503 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101697025 | TATCTCATTTTTAGT[A/G]GAGGCACTAAAACTT | 6468 |
rs186937561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666626 | GGTGAAGGAAGTGGA[C/T]GAAGATCCTAGGAAA | 6468 |
rs186952925 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615468 | CTGTGTGAGCCTGAT[C/G]AATGAGACACAGGCT | 6468 |
rs186956201 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616687 | CTGTTTTGGCGGCAG[C/G]TGGCAATCTGGTTTG | 6468 |
rs187106944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641521 | ATCTGACTATAGGAG[C/T]AAACTCAAATATTCT | 6468 |
rs187129963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101637119 | CCGGGCACGGTGGCT[C/T]ACATTTGCAATCCCA | 6468 |
rs187139211 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691101 | CTGGTCAAATCAAGT[C/T]TTGTGTAATGCTGAT | 6468 |
rs187223394 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101653996 | TGTGGTGGCATGCAT[C/T]TGTAATCCCAGCTAC | 6468 |
rs187255969 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677745 | GAGCAGTGATTCCAC[C/T]ACTGCACTCCAGCCT | 6468 |
rs187281202 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101620954 | CTTCACCAAGGCAAC[C/T]ATAGGCAGAAGAGGC | 6468 |
rs187331935 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669929 | CTGGCTAATTTTTTT[G/T]TATTTTTAGTAGACA | 6468 |
rs187382452 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672832 | AGACGATACTCTCAG[C/T]CAATCCTGAGACTCA | 6468 |
rs187386743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682490 | ATAAAGGAAGAAACT[A/G]TTTACAGTTATATCT | 6468 |
rs187389463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646590 | AGACTGTGAGGCAGC[C/T]GGGAAGGCCAGGGGA | 6468 |
rs187389683 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101623577 | AACACAGCATTTGTA[A/C]TCCTTGGCATTTATC | 6468 |
rs187573943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678404 | AAATTTGCTGGCCAG[A/G]GAGAGATACACTAAT | 6468 |
rs187668098 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101652109 | CATCTCCACCCCCTC[A/G]CTTCTCCTCACTCCG | 6468 |
rs187669687 | snp | A/C/G | 3.32535e-05 | 0.00407746 | intron-variant | FBXW4 | GRCh38.p7 | 10:101676461 | GACAGAACAGATAAT[A/C/G]CAATCACTACAACTT | 6468 |
rs187682619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628583 | GCTAGTCATGTGCAC[C/T]GTGAAGTTGGTCCCT | 6468 |
rs187695060 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101661855 | GTCAGCTACAGTCCA[C/T]GCCATCAGGAGGACC | 6468 |
rs187710355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654659 | TTAAATAAACTGTCA[C/T]ACTATTTTCTGACCT | 6468 |
rs187809224 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634791 | CCCATAAAGGTCTAA[G/T]AAAAAAATATAGGAA | 6468 |
rs187814429 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101610868 | GGTGAGGTCTGGCTG[A/G]TGCCAGGAGGCTATT | 6468 |
rs187834773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684426 | CCACTGCGCCTGGCC[C/T]ACCCAGCTAATTTTT | 6468 |
rs187842605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664319 | AATAGAAGAAAGAGA[C/T]AAATTGAGAAAAGAG | 6468 |
rs187905715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101638250 | CTGTGGTTTGTAAGG[C/T]GTGGAACTAGAATGC | 6468 |
rs187986517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684269 | GCTGGGACTACAGGC[A/G]CCCGCCACCATGCCC | 6468 |
rs188050250 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634080 | ATCGCACCACTGCAC[A/T]CCAGCCTGGGTAACA | 6468 |
rs188193623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632422 | AGCCAGAGAATGCCT[A/G]CAGAGAAACACAAAA | 6468 |
rs188245669 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641234 | TAAAAGCATGCACAA[C/T]TGGATAGGAGAATCT | 6468 |
rs188245807 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669806 | GTTGCCCAGGCTGGA[A/G]TGCAGTGGCGCAATA | 6468 |
rs188284559 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101690748 | AGAGGCTCTTCGTCC[C/G/T]GGAGTGCAGGCCATA | 6468 |
rs188326627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666944 | AAAAAACCACCCCAT[C/T]TCTAGGGCTGGGCAC | 6468 |
rs188328726 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629760 | GGGCTACACTTCAAG[A/G]GTTAGTCTTGTTTGA | 6468 |
rs188384972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101646734 | ACTACCCAGCAAATA[A/G]AGCCACAGGGAGAGG | 6468 |
rs188388878 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101613343 | AATCCCTGCAGCCAG[A/G]GGATGGGTGCAAGTA | 6468 |
rs188390834 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673222 | TTCTTCAGCACACCT[A/G]GGGCTGAACAGAGCT | 6468 |
rs188419108 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635683 | TTACAAAATATGAAA[A/G]AAATTAGCTGAGTGT | 6468 |
rs188429550 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695857 | CCCTCGTCACATGTG[G/T]CTGCTGAGCATTTGA | 6468 |
rs188473475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660615 | ATGTGATTGCTAAAT[C/T]ATCTGTTGGCAGAAC | 6468 |
rs188481691 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667797 | GCAACCTAGAATACA[C/G]AACAGGAAGATTTTC | 6468 |
rs188550468 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617402 | TTTGCAGGCTTTTCC[A/T]CCTCACAGATGCCCA | 6468 |
rs188623080 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101693701 | TATTTAACAGTTTAA[A/G]TGGTTCAGAAAAGTT | 6468 |
rs188751561 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668651 | AGGTTAAAAATATTG[C/G]TTGGAGCACATTATC | 6468 |
rs188765951 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640595 | TTCCTGGGTTCAAGC[A/G]ATTCTTGTGTCTTAG | 6468 |
rs188770433 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101618713 | CCACCCCTTTCCCCA[A/C]CCCACAATCCCAGTG | 6468 |
rs188771197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688589 | ACATGATTCAGGGTA[C/G]ATAAACATATTCTTA | 6468 |
rs188782010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640323 | AGTCTAGTCTTCAAG[G/T]GACAAGGCCCTGATC | 6468 |
rs188834088 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101692729 | CCAGCCCGGGCAACA[A/G]GAGTGAAACTCCGTC | 6468 |
rs188838190 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101645267 | GAACAGCCTCTTCTT[G/T]TTGGGGGGAAGCCCA | 6468 |
rs188899030 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626067 | ACAATAAAAATTGCA[C/G]GGCAGGTGTCTGCTC | 6468 |
rs188929618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101648741 | CCCTGTGTCTGCATT[C/T]CACCATTTTACCCTT | 6468 |
rs188983659 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622696 | TCACGCCACTGCACT[C/T]CAGCCTGGGCGACAT | 6468 |
rs189008766 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630724 | AAAGACACAGGCAGG[G/T]GGCAGGTGAAAGTGT | 6468 |
rs189036052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631581 | TCATTTTCCAAATAT[C/T]ATTTAATGAGCATGT | 6468 |
rs189079061 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101679374 | GCTCATAAAGAGCAA[C/T]TATAATTCTTATATT | 6468 |
rs189108636 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672421 | AAAGATGCAACAAAC[A/G]ACACCCCTCTCTCAT | 6468 |
rs189284365 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624276 | TTAGAAAGTTAAAAA[A/C]AAAAAAAAAACCAGA | 6468 |
rs189300722 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101665914 | GCGCACAGACCATCT[C/T]CGGCCCTGAGAGCTT | 6468 |
rs189587915 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689374 | CCATTCTTCCAGTTC[A/G]CATTTGGAGGTAGTG | 6468 |
rs189590318 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685697 | GAAACTTGCTTTTTT[A/T]AAAAAAAATGACATT | 6468 |
rs189594486 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | FBXW4 | GRCh38.p7 | 10:101656737 | TAAGCAGGCCCAGAG[A/G]CGAGCCTAAACACAA | 6468 |
rs189627850 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692314 | ATGTGTATATTATAT[A/G]TAATATATATATAAA | 6468 |
rs189635985 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672265 | GCTGTTGGGCACAAG[A/C]CTGGAGAAAGACTTC | 6468 |
rs189844031 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101680577 | TCACAATATAAAACA[C/T]TGGAGGAAACATCCC | 6468 |
rs189844266 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FBXW4 | GRCh38.p7 | 10:101631862 | TTGATCTCCTGACCT[C/T]GTGATCCACCCACCT | 6468 |
rs189924575 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101631689 | CTGGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT | 6468 |
rs189946646 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684754 | TGCATTAGCCTGAAT[A/C]TTCCAATAGCTTCAG | 6468 |
rs189957408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635205 | CTAGATTGTGGCTCC[G/T]TTTGAAAATCTAATG | 6468 |
rs189960552 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FBXW4 | GRCh38.p7 | 10:101639520 | AACTAGTAGACACCT[A/G]TTGTTCTGTGTGCCC | 6468 |
rs189964645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675312 | TTTTTGTGTTTAGAG[C/T]CATCTGGTAAACAGC | 6468 |
rs189977091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616795 | GCACAAACTCCGTGA[A/G]TGGCAGACAGCCATG | 6468 |
rs189997674 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667041 | TCGAGACCATCCTGG[C/T]TAACACAGTGAAACT | 6468 |
rs190077994 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101612161 | TTGGCTATAGCCAAG[A/C]CACTGGGACCAGGGC | 6468 |
rs190109730 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101642767 | AATAAAGGCCAAACA[C/T]ATCATGAGCCACAGG | 6468 |
rs190113774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621606 | AAAGAGACAGCTTGC[A/G]TTAGTTGAATGCCTC | 6468 |
rs190130761 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692013 | ATTTTCGGAAATACA[A/T]AGGAGTAAGTGCAAC | 6468 |
rs190153031 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101671215 | GGAGGGAAACCCAGG[A/C]AGCATCCGGAAAGCC | 6468 |
rs190212311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101665160 | TCTAATAATGAGGTA[A/G]AAAGACCCTATCCCA | 6468 |
rs190374836 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101641803 | TCACATTATTGTGTA[G/T]CAAAATAATATATGA | 6468 |
rs190388897 | snp | C/T | | | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101696400 | GGCTTTGCCCTAGAA[C/T]TACTTTTTGATCTTA | 6468 |
rs190471765 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647721 | AGAATGATAAGAAAG[C/G]TCACAAATTTGCAAA | 6468 |
rs190506892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101691497 | GAAATCAAAACACAC[A/G]TGTCTAATAAATAAT | 6468 |
rs190547762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101677128 | ATGGTACAGCCATTT[C/T]GGGAAAAGGTCTGGC | 6468 |
rs190703880 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101643780 | CCACACAATGAGTGG[A/G]AGGAGGAGAAACACT | 6468 |
rs190728207 | snp | A/C | | | intron-variant, downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101625388 | GGATGGGTATATGCT[A/C]CTACATAGGTGGGGC | 6468 |
rs190768348 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681421 | ATAATAATAATAATA[A/C]TACTAACAGGTCTAG | 6468 |
rs190885586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660066 | TCCTACCTGCCCCAT[A/G]GCCCAAAGGAAGGAA | 6468 |
rs190898578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632245 | GCAACCCTCTCTCAA[C/T]CCAAGTGCATCAGGG | 6468 |
rs190907775 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101627228 | TGCCTAGATGTGACA[A/T]CTATAAATGTTTCTT | 6468 |
rs190924592 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101682326 | TGTAGTCCCTGGTTT[A/T]AAATCACTATAGAGC | 6468 |
rs191004502 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622433 | ACCCTGTTAAGAGGA[C/T]AAAAAGACAAGCAGC | 6468 |
rs191010411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101658540 | ACAGTGCAAGACTTC[A/G]TCTGGGTGGCAGGGG | 6468 |
rs191047343 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666420 | GCTCTAATTCTTAGA[A/G]AGAAAAAAAATTGAA | 6468 |
rs191052288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101636125 | GAGGCTGAGGTGGGC[A/G]GATCAGTTGAGGTCA | 6468 |
rs191054400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101614734 | GCCCAGGACCCTCAA[G/T]GCTCTGTTGTGTGGT | 6468 |
rs191072968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101686364 | GAGAGGGAATGTGGC[A/G]CACAGCATTTTCCCC | 6468 |
rs191193342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634507 | AGAAGTTGTTCTACC[A/G]GATCAAAACATACTT | 6468 |
rs191199320 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | FBXW4 | GRCh38.p7 | 10:101610172 | CTGAGGCAGGAGAAT[C/T]GCTTCAACCTGGGAG | 6468 |
rs191218396 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101661313 | TCAGCACATGAGCCT[C/T]CCTGTGCCTATCCTG | 6468 |
rs191222993 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101662798 | CACTTCACCACATGC[A/C]CCCCATGGGTGGCTT | 6468 |
rs191288531 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101650990 | AAATCTCCCGCCTGG[A/G]CCCTGAGTTCGGCAG | 6468 |
rs191304791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688342 | TCATGTCAAATACCA[A/G]AAAAGAAGAGGAAGA | 6468 |
rs191452865 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101632917 | TTGCAGACAATATAA[G/T]TGTCTGCCTAGAAAA | 6468 |
rs191496017 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | FBXW4 | GRCh38.p7 | 10:101695900 | ACAAATTGAAATGAG[C/T]TATAAGTGAGAAATG | 6468 |
rs191504676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101687269 | ATATAATACCCCCTT[C/T]GGACTGCTCCCAACA | 6468 |
rs191563869 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101637166 | AGGCGGGCGGATCAC[C/G]AGGTCAGGAGATCAA | 6468 |
rs191596862 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FBXW4 | GRCh38.p7 | 10:101682869 | TCAATTTGGCTTTGA[A/C]TTGAAAAAGCTCTAC | 6468 |
rs191624505 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101669198 | AAACATACTAAGAGG[A/T]TCCTAAATGAGGAGG | 6468 |
rs191629018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640737 | TCCTGGCTGGTCTCA[C/T]GCTCCTGGCCTCAAG | 6468 |
rs191647709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101689506 | GCCTTTCCAAACGCC[A/G]AAGACAATAAATACA | 6468 |
rs191730137 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101621027 | GTGGTGTACCCAGCC[C/T]GCCACCCGGCTTGTG | 6468 |
rs191821761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101666703 | GAGGAGAGGGATTCT[A/G]TCTTGGTTCCAGAGA | 6468 |
rs191834555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101615733 | ATCACCATCTTTGTG[A/G]GGGCAGCTAACTGAT | 6468 |
rs191925045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101623809 | GGAATTATGCTGGGT[C/T]TTTAAAAAGCCAGTT | 6468 |
rs191941567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101694758 | CTCCTTCTTCCCATA[C/G]TCTCTTCCTTGTGCC | 6468 |
rs192001230 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101651344 | GGGTGGGAAATGGGT[A/G/T]GGGGGTGAAAGAAGG | 6468 |
rs192059014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653752 | TATAAGCTCCTACAC[A/G]GTAAAAACAAACAGT | 6468 |
rs192073331 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629060 | TATTCAAGTTGAGAG[A/G]TTAAAAATAACAAGA | 6468 |
rs192245042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101647368 | GGAGGAACTACTTGC[C/T]GGGTAGTTCTTTGAA | 6468 |
rs192298772 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101684433 | GCCTGGCCTACCCAG[A/C]TAATTTTTGTATGTT | 6468 |
rs192321769 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101664377 | TTCCTCCTAACTGCA[A/T]AAGGGAGCAACAAAG | 6468 |
rs192329669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101675732 | TTTGGTAGAGAGTCA[A/T]ATAATAACTATGAAA | 6468 |
rs192342030 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101628384 | CTAGTCCTTTCCATA[C/T]TCATGGGACAAATGG | 6468 |
rs192377729 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FBXW4 | GRCh38.p7 | 10:101634822 | AATAGTTTTATAATC[C/T]TGGAAAGACATTCTT | 6468 |
rs192537659 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678115 | GGCGAGTGTCAATAG[C/T]ACTTTCTGGGTGAGC | 6468 |
rs192617876 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101629761 | GGCTACACTTCAAGA[C/G]TTAGTCTTGTTTGAA | 6468 |
rs192653327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688522 | TCTAACAGGAGATAA[A/G]TTCTTTCTCCAGATA | 6468 |
rs192660445 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101630926 | CTCCAGAAGCTGCTC[A/G]AGTCACATCTGTGAT | 6468 |
rs192666817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624354 | ATTGTGAATAAAACC[C/T]GCATGTATTTTCACT | 6468 |
rs192670849 | snp | C/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101639811 | AGGATAAAGCCATGG[C/T]AGCACTATGGCCTCT | 6468 |
rs192672191 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667684 | GATGCTTAGGAAATT[C/T]GCATTTAGAAGGTTA | 6468 |
rs192749994 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673328 | CTTCTCCAGCTAACC[C/T]TATTAACTCCTTTTG | 6468 |
rs192856787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654258 | AATGTAAGGGAAGAT[A/C]TTCTGAAAGTGTTAG | 6468 |
rs192869748 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FBXW4 | GRCh38.p7 | 10:101688777 | AAAGTCAGTTTCTGC[A/G]GATCAAAGAAGGGAG | 6468 |
rs192878517 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FBXW4 | GRCh38.p7 | 10:101640479 | TCTTTTCTTTCTTTC[C/T]TTCTCTTTTTTTTTT | 6468 |
rs193029655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FBXW4 | GRCh38.p7 | 10:101622995 | GGCAAAAGACATGAA[C/T]AGACGTTTCGCCAAA | 6468 |
rs193040850 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101672438 | CACCCCTCTCTCATC[A/G]TCTCTGCTGCTTACT | 6468 |
rs193062123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101618383 | TTTATATTGAAGAGC[A/G]AGCAGGGTTTCATTA | 6468 |
rs193073481 | snp | A/C | 0.000592934 | 0.017208 | intron-variant | FBXW4 | GRCh38.p7 | 10:101667873 | AAACCACATCCAAAT[A/C]TGTCTCCCTTACCTG | 6468 |
rs193107775 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FBXW4 | GRCh38.p7 | 10:101617277 | TATGCTTCAGGGTGG[C/T]GGCACTCCCCACCTT | 6468 |
rs193150981 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101654672 | CATACTATTTTCTGA[A/C]CTTTTTTCATTCCAC | 6468 |
rs193208123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101692965 | ACTAGATTCTAACAT[A/C]TAAGACCCACAAAGA | 6468 |
rs193224290 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611045 | AGGGACGCAAGGCCC[A/G]GGTTCAGCCGCACTC | 6468 |
rs193226225 | snp | C/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101645936 | GTTTAGTTAGCCTCT[C/G]TTGGGTCTCAGTTTC | 6468 |
rs193302585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101678982 | CACAGGATAAAAAAA[A/C]ACACACACACAGATA | 6468 |
rs199504540 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101636121 | TTGGGAGGCTGAGGT[G/T]GGCGGATCAGTTGAG | 6468 |
rs199514450 | snp | C/G | 0.000115303 | 0.00759199 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101673543 | GGCAAACGTCCTCAT[C/G]ATGCCCAGCAAAGAC | 6468 |
rs199519506 | in-del | -/TA | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681399 | TCTCAAAAAAAAAAA[-/TA]ATAATAATAATAATA | 6468 |
rs199537021 | snp | A/G | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690354 | ATGAAACATTTCTTT[A/G]ATTTTTATTGTTATA | 6468 |
rs199557169 | in-del | -/T | 0.0539704 | 0.155153 | intron-variant | FBXW4 | GRCh38.p7 | 10:101626499 | AGACACAGGCATCTC[-/T]TTTTTTTTTTGAGAG | 6468 |
rs199576249 | snp | C/T | 0.000123364 | 0.00785283 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101612341 | AGCACACTCACCGGA[C/T]GCTGGTGCGGAGGTC | 6468 |
rs199587774 | snp | G/T | 1.76368e-05 | 0.00296953 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673690 | TGAAATGATGGAAAA[G/T]AAAATTTAAAAGTCA | 6468 |
rs199759905 | snp | A/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101627734 | GAGCCCACAAGATAG[A/T]TATTATTATTCCCAT | 6468 |
rs199799100 | snp | C/T | 6.60229e-05 | 0.00574518 | intron-variant | FBXW4 | GRCh38.p7 | 10:101668006 | GAGAGGAGATGCTCT[C/T]GTTGGCATTGCCTGG | 6468 |
rs199832357 | in-del | -/AT/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101681400 | CTCAAAAAAAAAAAA[-/AT/T]TAATAATAATAATAA | 6468 |
rs199851213 | snp | C/G | 1.64849e-05 | 0.00287092 | synonymous-codon, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611694 | GGAGGAACCTGTGGC[C/G]AGCAGGTGGTTGCCA | 6468 |
rs199871663 | snp | G/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101635275 | GACCATTTAGTTGCA[G/T]GAAAACAAGCTCAAG | 6468 |
rs199914852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101660660 | GAAAAACACAGGCAC[A/G]TTGCACACACAACCC | 6468 |
rs200082801 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101670594 | GCTCCCTGGCCAGGT[A/C]CGCACATCTCTTCTC | 6468 |
rs200162519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101616322 | CTCCTTCCTTCAGTC[A/G]AGCATCTTCTGTATA | 6468 |
rs200219849 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101678260 | TGAAGAGAATTTTGA[A/C]ATCATGAGCAAGAAT | 6468 |
rs200313671 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101629292 | TCCCTTTTTTTTTTT[-/T]GAGACAGAGTCTTGC | 6468 |
rs200345324 | snp | C/T | 0.000395309 | 0.0140534 | intron-variant | FBXW4 | GRCh38.p7 | 10:101624733 | GCCAGCATGGGCTCA[C/T]GAATCTCTTACCTGT | 6468 |
rs200395854 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101690465 | TCTTTGTGTCCCTTT[-/A]AAAAAAAAAGAAAAG | 6468 |
rs200410379 | snp | C/T | 0.000175171 | 0.00935708 | intron-variant | FBXW4 | GRCh38.p7 | 10:101612493 | CTGGGAAGGGAAGGA[C/T]GGAGTGAGAGGCTGC | 6468 |
rs200476624 | snp | C/T | 0.000396386 | 0.0140725 | missense, nc-transcript-variant | FBXW4 | GRCh38.p7 | 10:101611338 | TGTAAGACAGGGCAG[C/T]ATAGAGATGCTTGGT | 6468 |
rs200557925 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101640659 | ACCATCCCCAGCTAA[-/T]TTTTTTTTTTTTTTT | 6468 |
rs200687505 | in-del | -/A | 0.0146672 | 0.084371 | intron-variant | FBXW4 | GRCh38.p7 | 10:101641739 | AAGACATTTGAAGTT[-/A]GTAAATCAGAAATTA | 6468 |
rs200796259 | snp | A/G/T | 6.61303e-05 | 0.0057499 | intron-variant | FBXW4 | GRCh38.p7 | 10:101673461 | ATAAGATGGAAAAGG[A/G/T]TGGAAGGAGAAACCT | 6468 |
rs200903069 | snp | C/T | 6.61288e-05 | 0.00574979 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672906 | TATGTAAGGGGGAGA[C/T]CACCTCACCTTGGCC | 6468 |
rs200907900 | in-del | -/A | 0.0115144 | 0.0749975 | intron-variant | FBXW4 | GRCh38.p7 | 10:101685855 | CAAGCAAGAGTTTCC[-/A]AAAACATGGTCCTCC | 6468 |
rs200959342 | in-del | -/AAT | 0.474903 | 0.109173 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681719 | GAGACTCCGTCTCAA[-/AAT]AATAATAATAATAAT | 6468 |
rs200985549 | snp | A/T | 0.147656 | 0.228091 | intron-variant | FBXW4 | GRCh38.p7 | 10:101681401 | CTCAAAAAAAAAAAA[A/T]AATAATAATAATAAT | 6468 |
rs201061495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FBXW4 | GRCh38.p7 | 10:101672891 | AGGAGGGAGTAATAG[C/T]ATGTAAGGGGGAGAC | 6468 |
rs201180089 | in-del | -/AAAC | 0.0134861 | 0.0810011 | intron-variant | FBXW4 | GRCh38.p7 | 10:101653757 | GCTCCTACACGGTAA[-/AAAC]AAACAGTCTCTTGTG | 6468 |
rs201241363 | in-del | -/T | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101685691 | TTTTCTGAAACTTGC[-/T]TTTTTAAAAAAAAAT | 6468 |
rs201279739 | in-del | -/A | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101663637 | GCAAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGA | 6468 |
rs201339862 | snp | A/C | | | intron-variant | FBXW4 | GRCh38.p7 | 10:101674326 | AGAGGGAGACTGTCT[A/C]AAAAAAAAAAAAAAG | 6468 |
rs201433484 | in-del | -/A | 0.128632 | 0.218563 | intron-variant | FBXW4 | GRCh38.p7 | 10:101635450 | GCTATGGAAAAATTG[-/A]AAACTGTCTTCCATG | 6468 |